15-34531358-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531358
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531358
    reference: chr 15
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2413A>G
  hgvsp: ENSP00000452776.1:p.Ile805Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2263A>G
  hgvsp: ENSP00000387725.2:p.Ile755Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2440A>G
  hgvsp: ENSP00000346112.3:p.Ile814Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2440A>G
  hgvsp: ENSP00000453473.1:p.Ile814Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1876A>G
  hgvsp: ENSP00000390199.2:p.Ile626Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1876A>G
  hgvsp: ENSP00000452705.1:p.Ile626Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2440A>G
  hgvsp: ENSP00000454069.1:p.Ile814Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.388A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2287A>G
  hgvsp: ENSP00000290209.5:p.Ile763Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2440A>G
  hgvsp: ENSP00000454168.1:p.Ile814Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2440A>G
  hgvsp: ENSP00000453702.1:p.Ile814Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2263A>G
  hgvsp: ENSP00000380814.2:p.Ile755Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2395A>G
  hgvsp: ENSP00000380819.2:p.Ile799Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2263A>G
  hgvsp: ENSP00000452904.1:p.Ile755Val
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile814Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

15-34531361-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531361
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531361
    reference: chr 15
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873A>C
  hgvsp: ENSP00000452705.1:p.Thr625Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260A>C
  hgvsp: ENSP00000380814.2:p.Thr754Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873A>C
  hgvsp: ENSP00000390199.2:p.Thr625Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437A>C
  hgvsp: ENSP00000346112.3:p.Thr813Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392A>C
  hgvsp: ENSP00000380819.2:p.Thr798Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284A>C
  hgvsp: ENSP00000290209.5:p.Thr762Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437A>C
  hgvsp: ENSP00000453702.1:p.Thr813Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260A>C
  hgvsp: ENSP00000452904.1:p.Thr754Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437A>C
  hgvsp: ENSP00000454069.1:p.Thr813Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437A>C
  hgvsp: ENSP00000453473.1:p.Thr813Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410A>C
  hgvsp: ENSP00000452776.1:p.Thr804Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260A>C
  hgvsp: ENSP00000387725.2:p.Thr754Pro
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437A>C
  hgvsp: ENSP00000454168.1:p.Thr813Pro
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr813Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

15-34531368-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531368
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531368
    reference: chr 15
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-7C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-7C>G
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2437-7C>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

15-34531370-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531370
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531368
    reference: chr 15
allele count: 1
allele frequency: 8.267059076404159e-6
allele num: 120962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-11_2392-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-11_2437-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-11_2437-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-11_2410-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-11_2437-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-11_2437-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-11_2437-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-11_1873-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-11_2260-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-11_2260-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-11_2284-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-11_385-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-11_1873-10delGT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-11_2260-10delGT
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: GAC
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/15-34531380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531380
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531380
    reference: chr 15
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-19G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-19G>T
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

15-34531380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531380
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531380
    reference: chr 15
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-19G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-19G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

15-34531381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531381
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531381
    reference: chr 15
allele count: 2
allele frequency: 1.654423929587718e-5
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-20C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-20C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6834
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

15-34531383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531383
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531383
    reference: chr 15
allele count: 1
allele frequency: 8.272393368849475e-6
allele num: 120884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-22T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/15-34531399-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531399
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531399
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 120792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-38T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-38T>G
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-34531402-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531402
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531402
    reference: chr 15
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-41G>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-41G>T
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

15-34531404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531404
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531404
    reference: chr 15
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-43C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-43C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

15-34531405-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531405
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531405
    reference: chr 15
allele count: 6
allele frequency: 4.968532626697582e-5
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-44C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-44C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

15-34531407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531407
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531407
    reference: chr 15
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-46G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-46G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

15-34531408-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34531408
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34531408
    reference: chr 15
allele count: 2
allele frequency: 1.657824933687002e-5
allele num: 120640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2284-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2410-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2437-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1873-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2437-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2260-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.385-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2437-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2260-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2260-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2437-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2437-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1873-47T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2392-47T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

15-34532823-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532823
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532823
    reference: chr 15
allele count: 28
allele frequency: 2.30794592812397e-4
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+39C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+39C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

15-34532827-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532827
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532827
    reference: chr 15
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+35T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+35T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

15-34532835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532835
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532835
    reference: chr 15
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+27G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+27G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

15-34532840-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532840
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532840
    reference: chr 15
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+22T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+22T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum

15-34532850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532850
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532850
    reference: chr 15
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+12G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+12G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

15-34532850-CCTGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532850
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532846
    reference: chr 15
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+8_1872+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+8_2436+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+8_2283+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+8_2436+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+8_2436+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+8_2259+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+8_1872+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+8_2259+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+8_2436+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+8_2409+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+8_2391+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+8_2436+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+8_2259+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+8_384+11delTCAG
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2436+8_2436+11delTCAG
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: CCTGA
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

15-34532855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532855
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532855
    reference: chr 15
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+7G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+7G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2436+7G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/15-34532860-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532860
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532859
    reference: chr 15
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1872+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2409+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2436+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2436+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2259+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2391+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2259+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.384+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2259+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2436+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2436+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2436+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2283+1delG
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1872+1delG
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2436+1delG
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: AC
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

15-34532873-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532873
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532873
    reference: chr 15
allele count: 8
allele frequency: 6.589785831960461e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2425G>A
  hgvsp: ENSP00000454069.1:p.Ala809Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2248G>A
  hgvsp: ENSP00000380814.2:p.Ala750Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2248G>A
  hgvsp: ENSP00000387725.2:p.Ala750Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2398G>A
  hgvsp: ENSP00000452776.1:p.Ala800Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1861G>A
  hgvsp: ENSP00000452705.1:p.Ala621Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2272G>A
  hgvsp: ENSP00000290209.5:p.Ala758Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2425G>A
  hgvsp: ENSP00000453473.1:p.Ala809Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2380G>A
  hgvsp: ENSP00000380819.2:p.Ala794Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2425G>A
  hgvsp: ENSP00000453702.1:p.Ala809Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2425G>A
  hgvsp: ENSP00000454168.1:p.Ala809Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.373G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2425G>A
  hgvsp: ENSP00000346112.3:p.Ala809Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1861G>A
  hgvsp: ENSP00000390199.2:p.Ala621Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2248G>A
  hgvsp: ENSP00000452904.1:p.Ala750Thr
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala809Thr
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-34532879-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532879
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532879
    reference: chr 15
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1855G>A
  hgvsp: ENSP00000390199.2:p.Ala619Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2266G>A
  hgvsp: ENSP00000290209.5:p.Ala756Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1855G>A
  hgvsp: ENSP00000452705.1:p.Ala619Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2419G>A
  hgvsp: ENSP00000454069.1:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2392G>A
  hgvsp: ENSP00000452776.1:p.Ala798Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2419G>A
  hgvsp: ENSP00000453473.1:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2242G>A
  hgvsp: ENSP00000452904.1:p.Ala748Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.367G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2374G>A
  hgvsp: ENSP00000380819.2:p.Ala792Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2242G>A
  hgvsp: ENSP00000387725.2:p.Ala748Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2419G>A
  hgvsp: ENSP00000453702.1:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2419G>A
  hgvsp: ENSP00000454168.1:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2242G>A
  hgvsp: ENSP00000380814.2:p.Ala748Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2419G>A
  hgvsp: ENSP00000346112.3:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala807Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

15-34532886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532886
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532886
    reference: chr 15
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1848C>T
  hgvsp: ENST00000560164.1:c.1848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2412C>T
  hgvsp: ENST00000560611.1:c.2412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2412C>T
  hgvsp: ENST00000561080.1:c.2412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2412C>T
  hgvsp: ENST00000558667.1:c.2412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.360C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2259C>T
  hgvsp: ENST00000290209.5:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2235C>T
  hgvsp: ENST00000458406.2:c.2235C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2385C>T
  hgvsp: ENST00000558589.1:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2235C>T
  hgvsp: ENST00000559523.1:c.2235C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2235C>T
  hgvsp: ENST00000397702.2:c.2235C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2367C>T
  hgvsp: ENST00000397707.2:c.2367C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2412C>T
  hgvsp: ENST00000559664.1:c.2412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1848C>T
  hgvsp: ENST00000451844.2:c.1848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2412C>T
  hgvsp: ENST00000354181.3:c.2412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr804Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

15-34532889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532889
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532889
    reference: chr 15
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2409C>T
  hgvsp: ENST00000559664.1:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2382C>T
  hgvsp: ENST00000558589.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2256C>T
  hgvsp: ENST00000290209.5:c.2256C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2409C>T
  hgvsp: ENST00000558667.1:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.357C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2409C>T
  hgvsp: ENST00000354181.3:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2232C>T
  hgvsp: ENST00000559523.1:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2232C>T
  hgvsp: ENST00000458406.2:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2409C>T
  hgvsp: ENST00000561080.1:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2409C>T
  hgvsp: ENST00000560611.1:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1845C>T
  hgvsp: ENST00000451844.2:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1845C>T
  hgvsp: ENST00000560164.1:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2364C>T
  hgvsp: ENST00000397707.2:c.2364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2232C>T
  hgvsp: ENST00000397702.2:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn803Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-34532910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532910
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532910
    reference: chr 15
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2388C>T
  hgvsp: ENST00000558667.1:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2361C>T
  hgvsp: ENST00000558589.1:c.2361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2388C>T
  hgvsp: ENST00000561080.1:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2343C>T
  hgvsp: ENST00000397707.2:c.2343C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.336C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1824C>T
  hgvsp: ENST00000560164.1:c.1824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2235C>T
  hgvsp: ENST00000290209.5:c.2235C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2388C>T
  hgvsp: ENST00000560611.1:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2388C>T
  hgvsp: ENST00000559664.1:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2211C>T
  hgvsp: ENST00000458406.2:c.2211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2211C>T
  hgvsp: ENST00000559523.1:c.2211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1824C>T
  hgvsp: ENST00000451844.2:c.1824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2211C>T
  hgvsp: ENST00000397702.2:c.2211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2388C>T
  hgvsp: ENST00000354181.3:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile796Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

15-34532913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532913
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532913
    reference: chr 15
allele count: 32
allele frequency: 2.635827485091101e-4
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2208C>T
  hgvsp: ENST00000397702.2:c.2208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2232C>T
  hgvsp: ENST00000290209.5:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2385C>T
  hgvsp: ENST00000558667.1:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2385C>T
  hgvsp: ENST00000560611.1:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2208C>T
  hgvsp: ENST00000559523.1:c.2208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2385C>T
  hgvsp: ENST00000559664.1:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2385C>T
  hgvsp: ENST00000354181.3:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2358C>T
  hgvsp: ENST00000558589.1:c.2358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2208C>T
  hgvsp: ENST00000458406.2:c.2208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1821C>T
  hgvsp: ENST00000560164.1:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2385C>T
  hgvsp: ENST00000561080.1:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1821C>T
  hgvsp: ENST00000451844.2:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.333C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2340C>T
  hgvsp: ENST00000397707.2:c.2340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val795Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

15-34532916-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532916
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532916
    reference: chr 15
allele count: 8
allele frequency: 6.589677270555675e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2382T>C
  hgvsp: ENST00000561080.1:c.2382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2382T>C
  hgvsp: ENST00000560611.1:c.2382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2205T>C
  hgvsp: ENST00000397702.2:c.2205T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2382T>C
  hgvsp: ENST00000559664.1:c.2382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2205T>C
  hgvsp: ENST00000559523.1:c.2205T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2205T>C
  hgvsp: ENST00000458406.2:c.2205T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2382T>C
  hgvsp: ENST00000558667.1:c.2382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.330T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2229T>C
  hgvsp: ENST00000290209.5:c.2229T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2337T>C
  hgvsp: ENST00000397707.2:c.2337T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2355T>C
  hgvsp: ENST00000558589.1:c.2355T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2382T>C
  hgvsp: ENST00000354181.3:c.2382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1818T>C
  hgvsp: ENST00000560164.1:c.1818T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1818T>C
  hgvsp: ENST00000451844.2:c.1818T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser794Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS

15-34532926-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532926
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532926
    reference: chr 15
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.320T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2372T>C
  hgvsp: ENSP00000453473.1:p.Ile791Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2195T>C
  hgvsp: ENSP00000380814.2:p.Ile732Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2372T>C
  hgvsp: ENSP00000454069.1:p.Ile791Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2372T>C
  hgvsp: ENSP00000454168.1:p.Ile791Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1808T>C
  hgvsp: ENSP00000452705.1:p.Ile603Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2219T>C
  hgvsp: ENSP00000290209.5:p.Ile740Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2372T>C
  hgvsp: ENSP00000453702.1:p.Ile791Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2345T>C
  hgvsp: ENSP00000452776.1:p.Ile782Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2195T>C
  hgvsp: ENSP00000387725.2:p.Ile732Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2327T>C
  hgvsp: ENSP00000380819.2:p.Ile776Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1808T>C
  hgvsp: ENSP00000390199.2:p.Ile603Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2372T>C
  hgvsp: ENSP00000346112.3:p.Ile791Thr
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2195T>C
  hgvsp: ENSP00000452904.1:p.Ile732Thr
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile791Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-34532975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532975
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532975
    reference: chr 15
allele count: 5
allele frequency: 4.189218626941703e-5
allele num: 119354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.271C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2296C>T
  hgvsp: ENSP00000452776.1:p.Arg766Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2170C>T
  hgvsp: ENSP00000290209.5:p.Arg724Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1759C>T
  hgvsp: ENSP00000452705.1:p.Arg587Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2146C>T
  hgvsp: ENSP00000380814.2:p.Arg716Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2323C>T
  hgvsp: ENSP00000454168.1:p.Arg775Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2146C>T
  hgvsp: ENSP00000452904.1:p.Arg716Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2323C>T
  hgvsp: ENSP00000454069.1:p.Arg775Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2323C>T
  hgvsp: ENSP00000453702.1:p.Arg775Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2323C>T
  hgvsp: ENSP00000453473.1:p.Arg775Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2323C>T
  hgvsp: ENSP00000346112.3:p.Arg775Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2278C>T
  hgvsp: ENSP00000380819.2:p.Arg760Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2146C>T
  hgvsp: ENSP00000387725.2:p.Arg716Cys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1759C>T
  hgvsp: ENSP00000390199.2:p.Arg587Cys
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg775Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

15-34532982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532982
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532982
    reference: chr 15
allele count: 2
allele frequency: 1.687222662774806e-5
allele num: 118538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.264G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2289G>A
  hgvsp: ENST00000558589.1:c.2289G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1752G>A
  hgvsp: ENST00000560164.1:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2163G>A
  hgvsp: ENST00000290209.5:c.2163G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2139G>A
  hgvsp: ENST00000397702.2:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2316G>A
  hgvsp: ENST00000561080.1:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1752G>A
  hgvsp: ENST00000451844.2:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2316G>A
  hgvsp: ENST00000560611.1:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2316G>A
  hgvsp: ENST00000354181.3:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2316G>A
  hgvsp: ENST00000559664.1:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2316G>A
  hgvsp: ENST00000558667.1:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2139G>A
  hgvsp: ENST00000458406.2:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2271G>A
  hgvsp: ENST00000397707.2:c.2271G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2139G>A
  hgvsp: ENST00000559523.1:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys772Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/15-34532986-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532986
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532986
    reference: chr 15
allele count: 1
allele frequency: 8.494877588813945e-6
allele num: 117718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2135T>G
  hgvsp: ENSP00000387725.2:p.Val712Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2159T>G
  hgvsp: ENSP00000290209.5:p.Val720Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2135T>G
  hgvsp: ENSP00000380814.2:p.Val712Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2285T>G
  hgvsp: ENSP00000452776.1:p.Val762Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2312T>G
  hgvsp: ENSP00000453702.1:p.Val771Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2267T>G
  hgvsp: ENSP00000380819.2:p.Val756Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1748T>G
  hgvsp: ENSP00000390199.2:p.Val583Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2312T>G
  hgvsp: ENSP00000453473.1:p.Val771Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1748T>G
  hgvsp: ENSP00000452705.1:p.Val583Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2312T>G
  hgvsp: ENSP00000346112.3:p.Val771Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.260T>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2312T>G
  hgvsp: ENSP00000454069.1:p.Val771Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2135T>G
  hgvsp: ENSP00000452904.1:p.Val712Gly
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2312T>G
  hgvsp: ENSP00000454168.1:p.Val771Gly
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val771Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

15-34532994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532994
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532994
    reference: chr 15
allele count: 1
allele frequency: 8.669568082118148e-6
allele num: 115346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2127C>T
  hgvsp: ENST00000559523.1:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2277C>T
  hgvsp: ENST00000558589.1:c.2277C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2304C>T
  hgvsp: ENST00000558667.1:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2151C>T
  hgvsp: ENST00000290209.5:c.2151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.252C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2304C>T
  hgvsp: ENST00000560611.1:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2127C>T
  hgvsp: ENST00000397702.2:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2304C>T
  hgvsp: ENST00000561080.1:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2304C>T
  hgvsp: ENST00000559664.1:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2304C>T
  hgvsp: ENST00000354181.3:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2127C>T
  hgvsp: ENST00000458406.2:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1740C>T
  hgvsp: ENST00000451844.2:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1740C>T
  hgvsp: ENST00000560164.1:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2259C>T
  hgvsp: ENST00000397707.2:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp768Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

15-34532999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34532999
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34532999
    reference: chr 15
allele count: 1
allele frequency: 8.880363739698778e-6
allele num: 112608
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2299G>A
  hgvsp: ENSP00000346112.3:p.Glu767Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1735G>A
  hgvsp: ENSP00000452705.1:p.Glu579Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2122G>A
  hgvsp: ENSP00000380814.2:p.Glu708Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2299G>A
  hgvsp: ENSP00000454069.1:p.Glu767Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2299G>A
  hgvsp: ENSP00000453702.1:p.Glu767Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2299G>A
  hgvsp: ENSP00000454168.1:p.Glu767Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2299G>A
  hgvsp: ENSP00000453473.1:p.Glu767Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2146G>A
  hgvsp: ENSP00000290209.5:p.Glu716Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.247G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2272G>A
  hgvsp: ENSP00000452776.1:p.Glu758Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2254G>A
  hgvsp: ENSP00000380819.2:p.Glu752Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1735G>A
  hgvsp: ENSP00000390199.2:p.Glu579Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2122G>A
  hgvsp: ENSP00000387725.2:p.Glu708Lys
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2122G>A
  hgvsp: ENSP00000452904.1:p.Glu708Lys
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu767Lys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

15-34533005-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533005
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533005
    reference: chr 15
allele count: 1
allele frequency: 9.005925899241701e-6
allele num: 111038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2293C>G
  hgvsp: ENSP00000453473.1:p.Leu765Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2293C>G
  hgvsp: ENSP00000346112.3:p.Leu765Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.241C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2293C>G
  hgvsp: ENSP00000454069.1:p.Leu765Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2293C>G
  hgvsp: ENSP00000454168.1:p.Leu765Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2116C>G
  hgvsp: ENSP00000387725.2:p.Leu706Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2248C>G
  hgvsp: ENSP00000380819.2:p.Leu750Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2293C>G
  hgvsp: ENSP00000453702.1:p.Leu765Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2140C>G
  hgvsp: ENSP00000290209.5:p.Leu714Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2266C>G
  hgvsp: ENSP00000452776.1:p.Leu756Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1729C>G
  hgvsp: ENSP00000452705.1:p.Leu577Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2116C>G
  hgvsp: ENSP00000380814.2:p.Leu706Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1729C>G
  hgvsp: ENSP00000390199.2:p.Leu577Val
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2116C>G
  hgvsp: ENSP00000452904.1:p.Leu706Val
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu765Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

15-34533037-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533037
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533037
    reference: chr 15
allele count: 1
allele frequency: 1.07381397246741e-5
allele num: 93126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.209T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-7T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-7T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2268-7T>C
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

15-34533047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533047
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533047
    reference: chr 15
allele count: 1
allele frequency: 1.24470998257406e-5
allele num: 80340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.199C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-17C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-17C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

15-34533055-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533055
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533054
    reference: chr 15
allele count: 1
allele frequency: 1.401580983349218e-5
allele num: 71348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.190delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-26delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-26delT
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: GA
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

15-34533061-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533061
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533061
    reference: chr 15
allele count: 2
allele frequency: 3.058291026974127e-5
allele num: 65396
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.185T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-31T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-31T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD

15-34533063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533063
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533063
    reference: chr 15
allele count: 3
allele frequency: 4.6875e-5
allele num: 64000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.183C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-33C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-33C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7992
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19363
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

15-34533070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533070
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533070
    reference: chr 15
allele count: 5
allele frequency: 8.896797153024912e-5
allele num: 56200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.176G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-40G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-40G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15397
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

15-34533076-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533076
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533076
    reference: chr 15
allele count: 1
allele frequency: 1.983261274840348e-5
allele num: 50422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.170C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-46C>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-46C>G
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-34533077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533077
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533077
    reference: chr 15
allele count: 1
allele frequency: 2.020283647824155e-5
allele num: 49498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.169C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-47C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-47C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

15-34533080-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533080
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533080
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 46832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.166A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-50A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-50A>C
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

15-34533081-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533081
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533080
    reference: chr 15
allele count: 1
allele frequency: 2.159827213822894e-5
allele num: 46300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2115-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2091-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2223-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2268-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2268-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2091-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2241-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000558950
  gene symbol: SLC12A6
  hgvsc: ENST00000558950.1:n.164delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2268-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2091-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1704-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1704-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2268-52delC
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2268-52delC
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11223
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: TG
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

15-34533398-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533398
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533398
    reference: chr 15
allele count: 1
allele frequency: 9.590854161471621e-6
allele num: 104266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1703+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2222+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2267+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2267+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1703+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2090+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.416G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2267+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2240+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2090+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2114+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2090+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2267+36G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2267+36G>A
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14468
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

15-34533401-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533401
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533401
    reference: chr 15
allele count: 1
allele frequency: 9.486585967442037e-6
allele num: 105412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2240+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2090+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1703+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2090+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2267+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.413A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2114+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2267+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2267+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2090+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2267+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1703+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2222+33A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2267+33A>G
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

15-34533402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533402
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533402
    reference: chr 15
allele count: 1
allele frequency: 9.468620990039011e-6
allele num: 105612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2240+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2090+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2267+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1703+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1703+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2267+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2090+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.412C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2090+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2267+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2114+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2267+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2222+32C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2267+32C>T
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

15-34533415-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533415
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533415
    reference: chr 15
allele count: 1
allele frequency: 8.939266622566285e-6
allele num: 111866
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.399G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2114+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2090+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2267+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1703+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1703+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2240+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2090+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2222+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2267+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2267+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2267+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2090+19G>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2267+19G>C
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

15-34533417-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533417
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533417
    reference: chr 15
allele count: 1
allele frequency: 8.855042946958292e-6
allele num: 112930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2267+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1703+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2090+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2240+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2222+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.397T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2267+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2090+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2090+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2114+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2267+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2267+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2267+17T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1703+17T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

15-34533427-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533427
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533427
    reference: chr 15
allele count: 1
allele frequency: 8.553441905022582e-6
allele num: 116912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2240+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2267+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2222+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2267+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2090+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2267+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1703+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2267+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1703+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.387A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2114+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2267+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2090+7A>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2090+7A>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2267+7A>C
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

15-34533447-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533447
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533447
    reference: chr 15
allele count: 1
allele frequency: 8.321821480285606e-6
allele num: 120166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2254A>G
  hgvsp: ENSP00000454168.1:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2254A>G
  hgvsp: ENSP00000346112.3:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2227A>G
  hgvsp: ENSP00000452776.1:p.Thr743Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.367A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2101A>G
  hgvsp: ENSP00000290209.5:p.Thr701Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2254A>G
  hgvsp: ENSP00000453702.1:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2077A>G
  hgvsp: ENSP00000380814.2:p.Thr693Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2209A>G
  hgvsp: ENSP00000380819.2:p.Thr737Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1690A>G
  hgvsp: ENSP00000390199.2:p.Thr564Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2254A>G
  hgvsp: ENSP00000453473.1:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2254A>G
  hgvsp: ENSP00000454069.1:p.Thr752Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2077A>G
  hgvsp: ENSP00000452904.1:p.Thr693Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2077A>G
  hgvsp: ENSP00000387725.2:p.Thr693Ala
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1690A>G
  hgvsp: ENSP00000452705.1:p.Thr564Ala
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr752Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

15-34533468-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533468
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533468
    reference: chr 15
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2233T>C
  hgvsp: ENST00000559664.1:c.2233T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2188T>C
  hgvsp: ENST00000397707.2:c.2188T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1669T>C
  hgvsp: ENST00000560164.1:c.1669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2080T>C
  hgvsp: ENST00000290209.5:c.2080T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2233T>C
  hgvsp: ENST00000558667.1:c.2233T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2233T>C
  hgvsp: ENST00000560611.1:c.2233T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2233T>C
  hgvsp: ENST00000561080.1:c.2233T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2056T>C
  hgvsp: ENST00000559523.1:c.2056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2233T>C
  hgvsp: ENST00000354181.3:c.2233T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2056T>C
  hgvsp: ENST00000397702.2:c.2056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2206T>C
  hgvsp: ENST00000558589.1:c.2206T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2056T>C
  hgvsp: ENST00000458406.2:c.2056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1669T>C
  hgvsp: ENST00000451844.2:c.1669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.346T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu745Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

15-34533469-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533469
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533469
    reference: chr 15
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2205A>G
  hgvsp: ENST00000558589.1:c.2205A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1668A>G
  hgvsp: ENST00000451844.2:c.1668A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2232A>G
  hgvsp: ENST00000558667.1:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2187A>G
  hgvsp: ENST00000397707.2:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2232A>G
  hgvsp: ENST00000560611.1:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2055A>G
  hgvsp: ENST00000458406.2:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2079A>G
  hgvsp: ENST00000290209.5:c.2079A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2232A>G
  hgvsp: ENST00000354181.3:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2232A>G
  hgvsp: ENST00000559664.1:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2232A>G
  hgvsp: ENST00000561080.1:c.2232A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.345A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2055A>G
  hgvsp: ENST00000559523.1:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1668A>G
  hgvsp: ENST00000560164.1:c.1668A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2055A>G
  hgvsp: ENST00000397702.2:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg744Arg
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

15-34533471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533471
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533471
    reference: chr 15
allele count: 4
allele frequency: 3.302237265747544e-5
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2230C>T
  hgvsp: ENSP00000453702.1:p.Arg744Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2053C>T
  hgvsp: ENSP00000380814.2:p.Arg685Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2230C>T
  hgvsp: ENSP00000454168.1:p.Arg744Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1666C>T
  hgvsp: ENSP00000452705.1:p.Arg556Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2230C>T
  hgvsp: ENSP00000454069.1:p.Arg744Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2230C>T
  hgvsp: ENSP00000453473.1:p.Arg744Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2185C>T
  hgvsp: ENSP00000380819.2:p.Arg729Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2203C>T
  hgvsp: ENSP00000452776.1:p.Arg735Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2053C>T
  hgvsp: ENSP00000452904.1:p.Arg685Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2230C>T
  hgvsp: ENSP00000346112.3:p.Arg744Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2077C>T
  hgvsp: ENSP00000290209.5:p.Arg693Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.343C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1666C>T
  hgvsp: ENSP00000390199.2:p.Arg556Ter
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2053C>T
  hgvsp: ENSP00000387725.2:p.Arg685Ter
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg744Ter
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

15-34533486-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533486
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533486
    reference: chr 15
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2215C>T
  hgvsp: ENSP00000453702.1:p.Arg739Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1651C>T
  hgvsp: ENSP00000390199.2:p.Arg551Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2038C>T
  hgvsp: ENSP00000380814.2:p.Arg680Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2215C>T
  hgvsp: ENSP00000346112.3:p.Arg739Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2215C>T
  hgvsp: ENSP00000453473.1:p.Arg739Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2170C>T
  hgvsp: ENSP00000380819.2:p.Arg724Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1651C>T
  hgvsp: ENSP00000452705.1:p.Arg551Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2062C>T
  hgvsp: ENSP00000290209.5:p.Arg688Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2038C>T
  hgvsp: ENSP00000387725.2:p.Arg680Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2215C>T
  hgvsp: ENSP00000454168.1:p.Arg739Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2188C>T
  hgvsp: ENSP00000452776.1:p.Arg730Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2038C>T
  hgvsp: ENSP00000452904.1:p.Arg680Trp
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.328C>T
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2215C>T
  hgvsp: ENSP00000454069.1:p.Arg739Trp
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg739Trp
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

15-34533502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533502
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533502
    reference: chr 15
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2154G>A
  hgvsp: ENST00000397707.2:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2199G>A
  hgvsp: ENST00000559664.1:c.2199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.312G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2199G>A
  hgvsp: ENST00000560611.1:c.2199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2022G>A
  hgvsp: ENST00000458406.2:c.2022G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2172G>A
  hgvsp: ENST00000558589.1:c.2172G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1635G>A
  hgvsp: ENST00000560164.1:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2022G>A
  hgvsp: ENST00000397702.2:c.2022G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2199G>A
  hgvsp: ENST00000558667.1:c.2199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1635G>A
  hgvsp: ENST00000451844.2:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2022G>A
  hgvsp: ENST00000559523.1:c.2022G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2046G>A
  hgvsp: ENST00000290209.5:c.2046G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2199G>A
  hgvsp: ENST00000561080.1:c.2199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2199G>A
  hgvsp: ENST00000354181.3:c.2199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu733Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

15-34533505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533505
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533505
    reference: chr 15
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.2019G>A
  hgvsp: ENST00000559523.1:c.2019G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2151G>A
  hgvsp: ENST00000397707.2:c.2151G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2196G>A
  hgvsp: ENST00000560611.1:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.2019G>A
  hgvsp: ENST00000397702.2:c.2019G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1632G>A
  hgvsp: ENST00000560164.1:c.1632G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.309G>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2196G>A
  hgvsp: ENST00000561080.1:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2196G>A
  hgvsp: ENST00000558667.1:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1632G>A
  hgvsp: ENST00000451844.2:c.1632G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2043G>A
  hgvsp: ENST00000290209.5:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2196G>A
  hgvsp: ENST00000354181.3:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2196G>A
  hgvsp: ENST00000559664.1:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2169G>A
  hgvsp: ENST00000558589.1:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.2019G>A
  hgvsp: ENST00000458406.2:c.2019G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly732Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

15-34533542-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533542
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533542
    reference: chr 15
allele count: 1
allele frequency: 8.346548702111677e-6
allele num: 119810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2163-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.1986-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2163-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2010-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.276-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.1986-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2118-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2163-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2136-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1599-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2163-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2163-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1599-4A>G
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.1986-4A>G
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2163-4A>G
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

15-34533546-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533546
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533546
    reference: chr 15
allele count: 1
allele frequency: 8.385181706887589e-6
allele num: 119258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2163-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1599-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.276-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.1986-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2118-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2136-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2163-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.1986-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2163-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2163-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1599-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2163-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2010-8T>C
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.1986-8T>C
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2163-8T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

15-34533547-AAAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533547
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533543
    reference: chr 15
allele count: 1
allele frequency: 8.409155888931868e-6
allele num: 118918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2163-13_2163-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.1986-13_1986-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.276-13_276-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2136-13_2136-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2163-13_2163-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2010-13_2010-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1599-13_1599-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.1986-13_1986-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2163-13_2163-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1599-13_1599-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.1986-13_1986-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2163-13_2163-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2163-13_2163-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2118-13_2118-10delCTTT
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: AAAAG
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

15-34533549-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533549
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533549
    reference: chr 15
allele count: 1
allele frequency: 8.431845393682861e-6
allele num: 118598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2118-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2136-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.1986-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1599-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2163-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2163-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2163-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1599-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.1986-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.276-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.1986-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2163-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2010-11T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2163-11T>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-34533550-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533550
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533550
    reference: chr 15
allele count: 1
allele frequency: 8.501088139281828e-6
allele num: 117632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2163-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.276-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.1986-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.1986-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2163-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2118-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2010-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2163-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1599-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1599-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2136-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2163-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.1986-12T>A
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2163-12T>A
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

15-34533551-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34533551
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 34533550
    reference: chr 15
allele count: 26
allele frequency: 2.210809156151151e-4
allele num: 117604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000387725
  ensembl transcript: ENST00000458406
  gene symbol: SLC12A6
  hgvsc: ENST00000458406.2:c.1986-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000346112
  ensembl transcript: ENST00000354181
  gene symbol: SLC12A6
  hgvsc: ENST00000354181.3:c.2163-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380814
  ensembl transcript: ENST00000397702
  gene symbol: SLC12A6
  hgvsc: ENST00000397702.2:c.1986-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454168
  ensembl transcript: ENST00000560611
  gene symbol: SLC12A6
  hgvsc: ENST00000560611.1:c.2163-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl transcript: ENST00000560023
  gene symbol: SLC12A6
  hgvsc: ENST00000560023.1:n.276-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000290209
  ensembl transcript: ENST00000290209
  gene symbol: SLC12A6
  hgvsc: ENST00000290209.5:c.2010-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452705
  ensembl transcript: ENST00000560164
  gene symbol: SLC12A6
  hgvsc: ENST00000560164.1:c.1599-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000454069
  ensembl transcript: ENST00000561080
  gene symbol: SLC12A6
  hgvsc: ENST00000561080.1:c.2163-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452904
  ensembl transcript: ENST00000559523
  gene symbol: SLC12A6
  hgvsc: ENST00000559523.1:c.1986-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453473
  ensembl transcript: ENST00000558667
  gene symbol: SLC12A6
  hgvsc: ENST00000558667.1:c.2163-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000380819
  ensembl transcript: ENST00000397707
  gene symbol: SLC12A6
  hgvsc: ENST00000397707.2:c.2118-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000452776
  ensembl transcript: ENST00000558589
  gene symbol: SLC12A6
  hgvsc: ENST00000558589.1:c.2136-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000390199
  ensembl transcript: ENST00000451844
  gene symbol: SLC12A6
  hgvsc: ENST00000451844.2:c.1599-14delT
  variant of: http://identifiers.org/hgnc/10914
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140199
  ensembl protein: ENSP00000453702
  ensembl transcript: ENST00000559664
  gene symbol: SLC12A6
  hgvsc: ENST00000559664.1:c.2163-14delT
  variant of: http://identifiers.org/hgnc/10914
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 29702
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 2.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: GA
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ

GenotypeDepth
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1873
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7286
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 990
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7546
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5117
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2837
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3667
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3192
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3069
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37592
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.558e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.0586e1

VQSLOD
type: SiteQuality
SIO_000300: -1.266e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.659e0

MQRankSum
type: SiteQuality
SIO_000300: -4.46e-1

DP
type: SiteQuality
SIO_000300: 3.121246e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-1

GenotypeDepth
all individuals: 835
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2836
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7287
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1873
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5117
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1400
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2661
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6847
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1169
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7546
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5916
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37592
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503171692270691e-5
allele num: 66526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.12089e6

QD
type: SiteQuality
SIO_000300: 1.478e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2835
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6841
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2661
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7286
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1873
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1400
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1169
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5117
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1796
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5834
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37590
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503804625703029e-5
allele num: 66498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.236e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 5.629999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.027e0

DP
type: SiteQuality
SIO_000300: 3.119595e6

GenotypeDepth
all individuals: 6842
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3667
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3558
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2661
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2835
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 990
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3189
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37588
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.11941e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.706e1

FS
type: SiteQuality
SIO_000300: 8.942e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

MQ
type: SiteQuality
SIO_000300: 6.026e1

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeDepth
all individuals: 136
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2661
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1170
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5116
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6837
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7541
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37579
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 6.23e-1

MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: 2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

South Asian
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allele count: 1
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allele num: 16484
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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BaseQRankSum
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QD
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MQ
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SIO_000300: 5.975e1

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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SIO_000300: -8.500000000000001e-2

FS
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SIO_000300: 3.845e0

ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66450
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
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allele num: 11532
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 9.98e-1

VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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South Asian
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Other
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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Other
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South Asian
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African
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East Asian
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.531254707034192e-5
allele num: 66390
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66314
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.213886865744113e-4
allele num: 16476
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
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ReadPosRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.696147322510298e-3
allele num: 16508
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VQSLOD
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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DP
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SIO_000300: 1.901925e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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European (Non-Finnish)
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allele num: 66716
num of homozygotes: 0

South Asian
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Latino
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num of homozygotes: 0

European (Finnish)
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African
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East Asian
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Other
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.904506e6

VQSLOD
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SIO_000300: 6.0e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 5.15e0

ReadPosRankSum
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SIO_000300: 2.46e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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FS
type: SiteQuality
SIO_000300: 2.192e0

ClippingRankSum
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SIO_000300: 1.5e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 1.07e0

ClippingRankSum
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FS
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MQ
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MQRankSum
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BaseQRankSum
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SIO_000300: -3.638e0

InbreedingCoeff
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.905466e6

VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.273e0

QD
type: SiteQuality
SIO_000300: 1.237e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
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SIO_000300: -3.59e-1

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.93e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
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SIO_000300: -3.638e0

DP
type: SiteQuality
SIO_000300: 1.905466e6

ReadPosRankSum
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SIO_000300: 1.07e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.902e0

ClippingRankSum
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SIO_000300: 4.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.584e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.04e-1

ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.905586e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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SIO_000300: 1.33e-1

DP
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

Latino
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European (Finnish)
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allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele frequency: 1.498441620714457e-5
allele num: 66736
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MQRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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FS
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ReadPosRankSum
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SIO_000300: 2.19e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.905862e6

BaseQRankSum
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SIO_000300: -3.305e0

QD
type: SiteQuality
SIO_000300: 1.187e1

VQSLOD
type: SiteQuality
SIO_000300: 2.94e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.968e1

ReadPosRankSum
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ClippingRankSum
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QD
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DP
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SIO_000300: 1.905894e6

MQRankSum
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SIO_000300: 7.8e-2

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

ReadPosRankSum
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SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.905825e6

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.767e1

ClippingRankSum
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SIO_000300: -7.48e-1

QD
type: SiteQuality
SIO_000300: 1.089e1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -4.511e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
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allele count: 1
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allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.119e1

FS
type: SiteQuality
SIO_000300: 9.76e-1

DP
type: SiteQuality
SIO_000300: 1.905978e6

ReadPosRankSum
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SIO_000300: 9.17e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

ClippingRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -9.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.377e-1

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 18

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 32

European (Non-Finnish)
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allele count: 8
allele frequency: 1.19871737241152e-4
allele num: 66738
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

African
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South Asian
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allele num: 16512
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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East Asian
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European (Non-Finnish)
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allele count: 7
allele frequency: 1.04887770086008e-4
allele num: 66738
num of homozygotes: 0

South Asian
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Other
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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East Asian
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allele count: 0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: 6.18e0

FS
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DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 5.909e1

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.087168249330411e-5
allele num: 65712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.528584530724549e-4
allele num: 6542
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.99e-1

FS
type: SiteQuality
SIO_000300: 1.216e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.862247e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.67e1

ReadPosRankSum
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SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

BaseQRankSum
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SIO_000300: -2.243e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.065040152025992e-5
allele num: 65252
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
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SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.820000000000001e-1

DP
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SIO_000300: 1.839971e6

BaseQRankSum
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SIO_000300: -4.592e0

QD
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SIO_000300: 1.229e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 5.449e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.543162248078763e-5
allele num: 64802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.82018e6

FS
type: SiteQuality
SIO_000300: 3.665e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
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SIO_000300: 4.84e0

ClippingRankSum
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SIO_000300: -1.166e0

QD
type: SiteQuality
SIO_000300: 1.751e1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e-1

ReadPosRankSum
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SIO_000300: 1.33e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.574654363367241e-5
allele num: 63506
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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DP
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SIO_000300: 1.769885e6

FS
type: SiteQuality
SIO_000300: 6.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.569e-1

BaseQRankSum
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SIO_000300: -3.902e0

QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.72762645914397e-5
allele num: 10280
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.2e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.845e1

BaseQRankSum
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SIO_000300: -2.511e0

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.051303616484441e-4
allele num: 9512
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

InbreedingCoeff
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DP
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FS
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VQSLOD
type: SiteQuality
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 7.226477814713109e-5
allele num: 13838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51062
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.946e0

DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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SIO_000300: 1.356e1

MQ
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MQRankSum
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SIO_000300: -4.73e-1

BaseQRankSum
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SIO_000300: 1.57e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.288643749713919e-5
allele num: 43694
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.61e-1

ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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SIO_000300: -1.969e0

MQ
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SIO_000300: 5.752e1

InbreedingCoeff
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SIO_000300: -1.11e-2

FS
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.934e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38536
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.072109407376709e-4
allele num: 4826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4032
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
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SIO_000300: 1.069418e6

FS
type: SiteQuality
SIO_000300: 3.749e0

VQSLOD
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SIO_000300: 5.24e-1

ClippingRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 3.7e-2

MQRankSum
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SIO_000300: -5.0e-2

ReadPosRankSum
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SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 4.1e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.683109797681291e-5
allele num: 35192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.92e-2

MQRankSum
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SIO_000300: 9.5e-1

BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 8.217000000000001e0

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 8.702210361431803e-5
allele num: 34474
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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DP
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MQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.675940202453577e-4
allele num: 29834
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2904
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2292
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26438
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.019386106623587e-4
allele num: 4952
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.82e-2

QD
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ClippingRankSum
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FS
type: SiteQuality
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VQSLOD
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DP
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MQ
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BaseQRankSum
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SIO_000300: -2.113e0

ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.864286266326609e-5
allele num: 25878
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2652
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 24312
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 9.47913e5

MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.95e-2

ClippingRankSum
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FS
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SIO_000300: 3.641e0

VQSLOD
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SIO_000300: 6.04e-1

QD
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SIO_000300: 1.69e1

MQ
type: SiteQuality
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23938
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2442
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.9147332936744e-5
allele num: 10086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2860
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1948
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MQ
type: SiteQuality
SIO_000300: 6.228e1

InbreedingCoeff
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BaseQRankSum
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SIO_000300: -2.78e-1

ReadPosRankSum
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SIO_000300: -1.398e0

DP
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SIO_000300: 9.47302e5

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.25e0

QD
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SIO_000300: 1.23e1

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 56714
num of homozygotes: 0

East Asian
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Other
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MQRankSum
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DP
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.741796140179753e-5
allele num: 57412
num of homozygotes: 0

Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Latino
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VQSLOD
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FS
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 1.35464643727987e-4
allele num: 7382
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European (Finnish)
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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MQ
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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DP
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQ
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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European (Finnish)
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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South Asian
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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MQ
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 3.473428273706148e-4
allele num: 11516
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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VQSLOD
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QD
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DP
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.000570108320581e-5
allele num: 66654
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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African
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allele num: 10394
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Other
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 65878
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 65566
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Other
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4043
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529660109523664e-5
allele num: 65374
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.532e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.397e0

DP
type: SiteQuality
SIO_000300: 1.588758e6

VQSLOD
type: SiteQuality
SIO_000300: 9.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.92e-1

MQ
type: SiteQuality
SIO_000300: 5.716e1

GenotypeDepth
all individuals: 46
bin: 9.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 1

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65188
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.934432743890324e-5
allele num: 10066
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.586e1

FS
type: SiteQuality
SIO_000300: 1.0856e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.608e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.031e0

DP
type: SiteQuality
SIO_000300: 1.579517e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.502e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16100
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.954154727793696e-5
allele num: 11168
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
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SIO_000300: -2.477e0

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

QD
type: SiteQuality
SIO_000300: 9.68e0

DP
type: SiteQuality
SIO_000300: 1.53712e6

GenotypeDepth
all individuals: 157
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
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variant carriers: 0

GenotypeDepth
all individuals: 440
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1085
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1410
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 705
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 252
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
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variant carriers: 0

GenotypeQuality
all individuals: 4999
bin: 9.75e1
variant carriers: 26

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 4.025017028918199e-4
allele num: 64596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

QD
type: SiteQuality
SIO_000300: 1.222e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.005e1