14-92909080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909080
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909080
    reference: chr 14
allele count: 9
allele frequency: 7.413753336189001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.502G>A
  hgvsp: ENSP00000433302.1:p.Val168Ile
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.451G>A
  hgvsp: ENSP00000298877.1:p.Val151Ile
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000452099
  ensembl transcript: ENST00000554461
  gene symbol: SLC24A4
  hgvsc: ENST00000554461.1:c.175G>A
  hgvsp: ENSP00000452099.1:p.Val59Ile
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.502G>A
  hgvsp: ENSP00000431840.1:p.Val168Ile
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.451G>A
  hgvsp: ENSP00000337789.5:p.Val151Ile
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.155G>A
  hgvsp: ENSP00000432464.1:p.Val53Ile
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.310G>A
  hgvsp: ENSP00000376948.2:p.Val104Ile
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val168Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-92909080-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909080
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909080
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.155G>T
  hgvsp: ENSP00000432464.1:p.Val53Phe
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.502G>T
  hgvsp: ENSP00000431840.1:p.Val168Phe
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.451G>T
  hgvsp: ENSP00000298877.1:p.Val151Phe
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.502G>T
  hgvsp: ENSP00000433302.1:p.Val168Phe
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.451G>T
  hgvsp: ENSP00000337789.5:p.Val151Phe
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.310G>T
  hgvsp: ENSP00000376948.2:p.Val104Phe
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000452099
  ensembl transcript: ENST00000554461
  gene symbol: SLC24A4
  hgvsc: ENST00000554461.1:c.175G>T
  hgvsp: ENSP00000452099.1:p.Val59Phe
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val168Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

14-92909082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909082
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909082
    reference: chr 14
allele count: 5
allele frequency: 4.11868399808893e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000452099
  ensembl transcript: ENST00000554461
  gene symbol: SLC24A4
  hgvsc: ENST00000554461.1:c.177C>T
  hgvsp: ENST00000554461.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.453C>T
  hgvsp: ENST00000298877.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.504C>T
  hgvsp: ENST00000531433.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.157C>T
  hgvsp: ENST00000525557.1:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.312C>T
  hgvsp: ENST00000393265.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.504C>T
  hgvsp: ENST00000532405.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.453C>T
  hgvsp: ENST00000351924.5:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23936
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val168Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

14-92909091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909091
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909091
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.321C>T
  hgvsp: ENST00000393265.2:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.513C>T
  hgvsp: ENST00000531433.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.462C>T
  hgvsp: ENST00000298877.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.462C>T
  hgvsp: ENST00000351924.5:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.513C>T
  hgvsp: ENST00000532405.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.166C>T
  hgvsp: ENST00000525557.1:c.166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000452099
  ensembl transcript: ENST00000554461
  gene symbol: SLC24A4
  hgvsc: ENST00000554461.1:c.186C>T
  hgvsp: ENST00000554461.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23997
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly171Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

14-92909097-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909097
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909097
    reference: chr 14
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.468C>G
  hgvsp: ENSP00000337789.5:p.Ile156Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.327C>G
  hgvsp: ENSP00000376948.2:p.Ile109Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.519C>G
  hgvsp: ENSP00000433302.1:p.Ile173Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.519C>G
  hgvsp: ENSP00000431840.1:p.Ile173Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.468C>G
  hgvsp: ENSP00000298877.1:p.Ile156Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000452099
  ensembl transcript: ENST00000554461
  gene symbol: SLC24A4
  hgvsc: ENST00000554461.1:c.192C>G
  hgvsp: ENSP00000452099.1:p.Ile64Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.172C>G
  hgvsp: ENSP00000432464.1:p.Ile58Met
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3760
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2501
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8907
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile173Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

14-92909098-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909098
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909098
    reference: chr 14
allele count: 6
allele frequency: 4.942583653228331e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.328G>A
  hgvsp: ENSP00000376948.2:p.Val110Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.469G>A
  hgvsp: ENSP00000298877.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.173G>A
  hgvsp: ENSP00000432464.1:p.Val59Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.469G>A
  hgvsp: ENSP00000337789.5:p.Val157Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.520G>A
  hgvsp: ENSP00000431840.1:p.Val174Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.520G>A
  hgvsp: ENSP00000433302.1:p.Val174Met
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11603
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 24020
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8909
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val174Met
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

14-92909102-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909102
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909102
    reference: chr 14
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.524G>T
  hgvsp: ENSP00000431840.1:p.Gly175Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.524G>T
  hgvsp: ENSP00000433302.1:p.Gly175Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.332G>T
  hgvsp: ENSP00000376948.2:p.Gly111Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.177G>T
  hgvsp: ENSP00000432464.1:p.Gly60Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.473G>T
  hgvsp: ENSP00000337789.5:p.Gly158Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.473G>T
  hgvsp: ENSP00000298877.1:p.Gly158Val
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4796
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24028
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly175Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

14-92909103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909103
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909103
    reference: chr 14
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.178C>T
  hgvsp: ENST00000525557.1:c.178C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.525C>T
  hgvsp: ENST00000532405.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.333C>T
  hgvsp: ENST00000393265.2:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.525C>T
  hgvsp: ENST00000531433.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.474C>T
  hgvsp: ENST00000351924.5:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.474C>T
  hgvsp: ENST00000298877.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11595
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8906
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24030
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly175Gly
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

14-92909118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909118
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909118
    reference: chr 14
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.540C>T
  hgvsp: ENST00000531433.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.348C>T
  hgvsp: ENST00000393265.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.489C>T
  hgvsp: ENST00000351924.5:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.489C>T
  hgvsp: ENST00000298877.1:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.540C>T
  hgvsp: ENST00000532405.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.193C>T
  hgvsp: ENST00000525557.1:c.193C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn180Asn
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

14-92909127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909127
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909127
    reference: chr 14
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.498C>T
  hgvsp: ENST00000351924.5:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.549C>T
  hgvsp: ENST00000532405.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.549C>T
  hgvsp: ENST00000531433.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.498C>T
  hgvsp: ENST00000298877.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.202C>T
  hgvsp: ENST00000525557.1:c.202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.357C>T
  hgvsp: ENST00000393265.2:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys183Cys
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

14-92909142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909142
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909142
    reference: chr 14
allele count: 505
allele frequency: 4.161790641327818e-3
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.217C>T
  hgvsp: ENST00000525557.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.513C>T
  hgvsp: ENST00000298877.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.372C>T
  hgvsp: ENST00000393265.2:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.564C>T
  hgvsp: ENST00000531433.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.564C>T
  hgvsp: ENST00000532405.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.513C>T
  hgvsp: ENST00000351924.5:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 15940
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 9.75e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18782
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 23985
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11608
  bin: 9.75e1
  variant carriers: 496
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys188Cys
num of homozygotes: 9
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-92909143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909143
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909143
    reference: chr 14
allele count: 10
allele frequency: 8.241577108195424e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.514G>A
  hgvsp: ENSP00000298877.1:p.Gly172Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.373G>A
  hgvsp: ENSP00000376948.2:p.Gly125Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.565G>A
  hgvsp: ENSP00000433302.1:p.Gly189Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.565G>A
  hgvsp: ENSP00000431840.1:p.Gly189Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.514G>A
  hgvsp: ENSP00000337789.5:p.Gly172Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.218G>A
  hgvsp: ENSP00000432464.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly189Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

14-92909143-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909143
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909143
    reference: chr 14
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.218G>T
  hgvsp: ENSP00000432464.1:p.Gly74Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.565G>T
  hgvsp: ENSP00000431840.1:p.Gly189Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.373G>T
  hgvsp: ENSP00000376948.2:p.Gly125Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.514G>T
  hgvsp: ENSP00000298877.1:p.Gly172Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.514G>T
  hgvsp: ENSP00000337789.5:p.Gly172Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.565G>T
  hgvsp: ENSP00000433302.1:p.Gly189Ter
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4812
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3413
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly189Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/14-92909159-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909159
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909159
    reference: chr 14
allele count: 16
allele frequency: 1.319848877303549e-4
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.581A>C
  hgvsp: ENSP00000433302.1:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.581A>C
  hgvsp: ENSP00000431840.1:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.234A>C
  hgvsp: ENSP00000432464.1:p.Gln79Pro
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.530A>C
  hgvsp: ENSP00000298877.1:p.Gln177Pro
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.389A>C
  hgvsp: ENSP00000376948.2:p.Gln130Pro
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.530A>C
  hgvsp: ENSP00000337789.5:p.Gln177Pro
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23983
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln194Pro
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-92909159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909159
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909159
    reference: chr 14
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.389A>G
  hgvsp: ENSP00000376948.2:p.Gln130Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.530A>G
  hgvsp: ENSP00000337789.5:p.Gln177Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.530A>G
  hgvsp: ENSP00000298877.1:p.Gln177Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.234A>G
  hgvsp: ENSP00000432464.1:p.Gln79Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.581A>G
  hgvsp: ENSP00000431840.1:p.Gln194Arg
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.581A>G
  hgvsp: ENSP00000433302.1:p.Gln194Arg
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln194Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

14-92909174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909174
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909174
    reference: chr 14
allele count: 2
allele frequency: 1.652510162937502e-5
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+14C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11195
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4709
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8633
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 2.25e1
  variant carriers: 0
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: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-92909183-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909183
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909183
    reference: chr 14
allele count: 2
allele frequency: 1.655629139072848e-5
allele num: 120800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+23C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+23C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+23C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+23C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+23C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+23C>G
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11146
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8339
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22065
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
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: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

14-92909183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909183
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909183
    reference: chr 14
allele count: 5
allele frequency: 4.139072847682119e-5
allele num: 120800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+23C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+23C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+23C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+23C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+23C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+23C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-92909184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909184
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909184
    reference: chr 14
allele count: 2
allele frequency: 1.655135886656295e-5
allele num: 120836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+24G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+24G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+24G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+24G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+24G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+24G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14819
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3186
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

14-92909186-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909186
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909184
    reference: chr 14
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+28_531+29delGA
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+28_582+29delGA
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+28_390+29delGA
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+28_582+29delGA
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+28_531+29delGA
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+28_235+29delGA
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11119
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21717
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4498
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3145
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: CAG
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

14-92909205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909205
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909205
    reference: chr 14
allele count: 1
allele frequency: 8.314210648840998e-6
allele num: 120276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+45G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+45G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+45G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+45G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+45G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+45G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-92909207-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909207
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909207
    reference: chr 14
allele count: 1
allele frequency: 8.323622440486099e-6
allele num: 120140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+47G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+47G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+47G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+47G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+47G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+47G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3455
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

14-92909211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909211
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909211
    reference: chr 14
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+51G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+51G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+51G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+51G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+51G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+51G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9600
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2682
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11054
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

14-92909212-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909212
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909212
    reference: chr 14
allele count: 2
allele frequency: 1.67000668002672e-5
allele num: 119760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.390+52A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.582+52A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.531+52A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.531+52A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.582+52A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.235+52A>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11737
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11058
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4717
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

14-92909700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909700
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909700
    reference: chr 14
allele count: 10543
allele frequency: 9.19741777894094e-2
allele num: 114630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-44C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-44C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-44C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-44C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-44C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-44C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14520
  bin: 2.25e1
  variant carriers: 1933
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.25e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 10527
  bin: 2.75e1
  variant carriers: 1513
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 378
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 3.25e1
  variant carriers: 1060
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 7.5e0
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 1.25e1
  variant carriers: 864
genotype depth: GenotypeDepth
  all individuals: 9498
  bin: 1.75e1
  variant carriers: 1698
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.75e1
  variant carriers: 803
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.75e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 4.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 8.25e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 6.75e1
  variant carriers: 78
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 5.25e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.5e0
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 13961
  bin: 9.75e1
  variant carriers: 9030
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 7.75e1
  variant carriers: 82
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 1.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 14644
  bin: 6.25e1
  variant carriers: 83
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 4.25e1
  variant carriers: 39
num of homozygotes: 832
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

14-92909701-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909701
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909701
    reference: chr 14
allele count: 3
allele frequency: 2.599067801015369e-5
allele num: 115426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-43G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-43G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-43G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-43G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-43G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-43G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11226
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1958
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2670
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3269
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19205
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

14-92909708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909708
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909708
    reference: chr 14
allele count: 5
allele frequency: 4.326082818529478e-5
allele num: 115578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-36C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-36C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-36C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-36C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-36C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-36C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25369
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6634
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

14-92909709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909709
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909709
    reference: chr 14
allele count: 93
allele frequency: 8.010749909556049e-4
allele num: 116094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-35G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-35G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-35G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-35G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.1G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-35G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-35G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 21013
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26552
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2953
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6730
  bin: 9.75e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 2424
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

14-92909723-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909723
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909723
    reference: chr 14
allele count: 2
allele frequency: 1.696957355461657e-5
allele num: 117858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.15A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-21A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-21A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-21A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-21A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-21A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-21A>G
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6655
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-92909724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909724
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909724
    reference: chr 14
allele count: 3
allele frequency: 2.544874622510264e-5
allele num: 117884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.16C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-20C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25147
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2036
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32765
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

14-92909725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909725
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909725
    reference: chr 14
allele count: 2
allele frequency: 1.692792091275349e-5
allele num: 118148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-19G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-19G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-19G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-19G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.17G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-19G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-19G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14603
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

14-92909727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909727
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909727
    reference: chr 14
allele count: 5
allele frequency: 4.225542559664661e-5
allele num: 118328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.19C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-17C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6655
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

14-92909728-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909728
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909728
    reference: chr 14
allele count: 295
allele frequency: 2.489829678769771e-3
allele num: 118482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-16G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-16G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.20G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-16G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-16G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-16G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-16G>C
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25743
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 14859
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6864
  bin: 9.75e1
  variant carriers: 289
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 3
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-92909730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909730
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909730
    reference: chr 14
allele count: 1
allele frequency: 8.422896802668375e-6
allele num: 118724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-14G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-14G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.22G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-14G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-14G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-14G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-14G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6667
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

14-92909735-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909735
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909735
    reference: chr 14
allele count: 1
allele frequency: 8.389824820457749e-6
allele num: 119192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-9T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-9T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-9T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-9T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.27T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-9T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-9T>G
  variant of: http://identifiers.org/hgnc/10978
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6532
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

14-92909738-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909738
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909738
    reference: chr 14
allele count: 1
allele frequency: 8.3760511944249e-6
allele num: 119388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-6T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.30T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-6T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-6T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-6T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-6T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-6T>C
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
hgvs: c.583-6T>C
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

14-92909739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909739
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909739
    reference: chr 14
allele count: 1
allele frequency: 8.369741709770836e-6
allele num: 119478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.31G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.532-5G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.236-5G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.391-5G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.583-5G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.583-5G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.532-5G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6664
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
hgvs: c.583-5G>A
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

14-92909745-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909745
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909745
    reference: chr 14
allele count: 10
allele frequency: 8.396587626788474e-5
allele num: 119096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.533T>G
  hgvsp: ENSP00000337789.5:p.Val178Gly
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.37T>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.584T>G
  hgvsp: ENSP00000431840.1:p.Val195Gly
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.392T>G
  hgvsp: ENSP00000376948.2:p.Val131Gly
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.584T>G
  hgvsp: ENSP00000433302.1:p.Val195Gly
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.533T>G
  hgvsp: ENSP00000298877.1:p.Val178Gly
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.237T>G
  hgvsp: ENSP00000432464.1:p.Val80Gly
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26124
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val195Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/14-92909750-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909750
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909750
    reference: chr 14
allele count: 1
allele frequency: 8.321544478655239e-6
allele num: 120170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.397C>A
  hgvsp: ENSP00000376948.2:p.Arg133Ser
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.589C>A
  hgvsp: ENSP00000431840.1:p.Arg197Ser
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.538C>A
  hgvsp: ENSP00000337789.5:p.Arg180Ser
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.589C>A
  hgvsp: ENSP00000433302.1:p.Arg197Ser
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.538C>A
  hgvsp: ENSP00000298877.1:p.Arg180Ser
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.242C>A
  hgvsp: ENSP00000432464.1:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.42C>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2881
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg197Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

14-92909750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909750
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909750
    reference: chr 14
allele count: 8
allele frequency: 6.657235582924191e-5
allele num: 120170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.589C>T
  hgvsp: ENSP00000433302.1:p.Arg197Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.589C>T
  hgvsp: ENSP00000431840.1:p.Arg197Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.538C>T
  hgvsp: ENSP00000298877.1:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.242C>T
  hgvsp: ENSP00000432464.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.538C>T
  hgvsp: ENSP00000337789.5:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.397C>T
  hgvsp: ENSP00000376948.2:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.42C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2881
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36121
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg197Cys
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

14-92909751-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909751
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909751
    reference: chr 14
allele count: 3
allele frequency: 2.495632642874969e-5
allele num: 120210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.43G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.398G>A
  hgvsp: ENSP00000376948.2:p.Arg133His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.590G>A
  hgvsp: ENSP00000431840.1:p.Arg197His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.539G>A
  hgvsp: ENSP00000337789.5:p.Arg180His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.590G>A
  hgvsp: ENSP00000433302.1:p.Arg197His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.539G>A
  hgvsp: ENSP00000298877.1:p.Arg180His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.243G>A
  hgvsp: ENSP00000432464.1:p.Arg82His
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26333
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6662
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg197His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

14-92909751-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909751
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909751
    reference: chr 14
allele count: 1
allele frequency: 8.318775476249896e-6
allele num: 120210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.590G>T
  hgvsp: ENSP00000433302.1:p.Arg197Leu
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.43G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.243G>T
  hgvsp: ENSP00000432464.1:p.Arg82Leu
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.398G>T
  hgvsp: ENSP00000376948.2:p.Arg133Leu
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.539G>T
  hgvsp: ENSP00000337789.5:p.Arg180Leu
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.590G>T
  hgvsp: ENSP00000431840.1:p.Arg197Leu
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.539G>T
  hgvsp: ENSP00000298877.1:p.Arg180Leu
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6662
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg197Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-92909752-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909752
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909752
    reference: chr 14
allele count: 12
allele frequency: 9.979044007584074e-5
allele num: 120252
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.591T>C
  hgvsp: ENST00000532405.1:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.399T>C
  hgvsp: ENST00000393265.2:c.399T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.44T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.540T>C
  hgvsp: ENST00000351924.5:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.591T>C
  hgvsp: ENST00000531433.1:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.244T>C
  hgvsp: ENST00000525557.1:c.244T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.540T>C
  hgvsp: ENST00000298877.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16030
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26353
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg197Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

14-92909757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909757
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909757
    reference: chr 14
allele count: 4
allele frequency: 3.32242470555011e-5
allele num: 120394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.404C>T
  hgvsp: ENSP00000376948.2:p.Thr135Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.596C>T
  hgvsp: ENSP00000433302.1:p.Thr199Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.249C>T
  hgvsp: ENSP00000432464.1:p.Thr84Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.545C>T
  hgvsp: ENSP00000298877.1:p.Thr182Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.596C>T
  hgvsp: ENSP00000431840.1:p.Thr199Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.545C>T
  hgvsp: ENSP00000337789.5:p.Thr182Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.49C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6696
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr199Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-92909758-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909758
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909758
    reference: chr 14
allele count: 4
allele frequency: 3.321155762205247e-5
allele num: 120440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.250G>A
  hgvsp: ENST00000525557.1:c.250G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.405G>A
  hgvsp: ENST00000393265.2:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.50G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.546G>A
  hgvsp: ENST00000351924.5:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.597G>A
  hgvsp: ENST00000531433.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.597G>A
  hgvsp: ENST00000532405.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.546G>A
  hgvsp: ENST00000298877.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36474
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr199Thr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

14-92909761-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909761
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909761
    reference: chr 14
allele count: 1
allele frequency: 8.297791128001726e-6
allele num: 120514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.600G>C
  hgvsp: ENSP00000433302.1:p.Trp200Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.53G>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.549G>C
  hgvsp: ENSP00000298877.1:p.Trp183Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.253G>C
  hgvsp: ENSP00000432464.1:p.Trp85Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.600G>C
  hgvsp: ENSP00000431840.1:p.Trp200Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.408G>C
  hgvsp: ENSP00000376948.2:p.Trp136Cys
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.549G>C
  hgvsp: ENSP00000337789.5:p.Trp183Cys
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp200Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

14-92909765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909765
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909765
    reference: chr 14
allele count: 2
allele frequency: 1.6583472910897e-5
allele num: 120602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.412G>A
  hgvsp: ENSP00000376948.2:p.Ala138Thr
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.604G>A
  hgvsp: ENSP00000433302.1:p.Ala202Thr
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.257G>A
  hgvsp: ENSP00000432464.1:p.Ala87Thr
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.57G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.553G>A
  hgvsp: ENSP00000298877.1:p.Ala185Thr
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.553G>A
  hgvsp: ENSP00000337789.5:p.Ala185Thr
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.604G>A
  hgvsp: ENSP00000431840.1:p.Ala202Thr
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6661
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 36686
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala202Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

14-92909767-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909767
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909767
    reference: chr 14
allele count: 4
allele frequency: 3.315045333244932e-5
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.414C>T
  hgvsp: ENST00000393265.2:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.555C>T
  hgvsp: ENST00000351924.5:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.606C>T
  hgvsp: ENST00000532405.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.259C>T
  hgvsp: ENST00000525557.1:c.259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.59C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.555C>T
  hgvsp: ENST00000298877.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.606C>T
  hgvsp: ENST00000531433.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala202Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

14-92909768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909768
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909768
    reference: chr 14
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.60G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.607G>A
  hgvsp: ENSP00000431840.1:p.Val203Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.556G>A
  hgvsp: ENSP00000298877.1:p.Val186Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.260G>A
  hgvsp: ENSP00000432464.1:p.Val88Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.607G>A
  hgvsp: ENSP00000433302.1:p.Val203Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.556G>A
  hgvsp: ENSP00000337789.5:p.Val186Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.415G>A
  hgvsp: ENSP00000376948.2:p.Val139Met
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36830
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2885
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val203Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-92909774-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909774
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909774
    reference: chr 14
allele count: 2
allele frequency: 1.655574318731168e-5
allele num: 120804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.421C>A
  hgvsp: ENST00000393265.2:c.421C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.562C>A
  hgvsp: ENST00000298877.1:c.562C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.266C>A
  hgvsp: ENST00000525557.1:c.266C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.613C>A
  hgvsp: ENST00000531433.1:c.613C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.562C>A
  hgvsp: ENST00000351924.5:c.562C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.613C>A
  hgvsp: ENST00000532405.1:c.613C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.66C>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36962
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6661
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2887
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg205Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

14-92909774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909774
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909774
    reference: chr 14
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.562C>T
  hgvsp: ENSP00000337789.5:p.Arg188Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.266C>T
  hgvsp: ENSP00000432464.1:p.Arg90Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.66C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.613C>T
  hgvsp: ENSP00000433302.1:p.Arg205Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.562C>T
  hgvsp: ENSP00000298877.1:p.Arg188Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.613C>T
  hgvsp: ENSP00000431840.1:p.Arg205Ter
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.421C>T
  hgvsp: ENSP00000376948.2:p.Arg141Ter
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36962
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg205Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-92909775-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909775
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909775
    reference: chr 14
allele count: 2
allele frequency: 1.655437283758505e-5
allele num: 120814
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.563G>A
  hgvsp: ENSP00000337789.5:p.Arg188Gln
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.614G>A
  hgvsp: ENSP00000433302.1:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.267G>A
  hgvsp: ENSP00000432464.1:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.422G>A
  hgvsp: ENSP00000376948.2:p.Arg141Gln
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.614G>A
  hgvsp: ENSP00000431840.1:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.563G>A
  hgvsp: ENSP00000298877.1:p.Arg188Gln
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.67G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg205Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

14-92909782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909782
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909782
    reference: chr 14
allele count: 1
allele frequency: 8.272530236098013e-6
allele num: 120882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.570C>T
  hgvsp: ENST00000351924.5:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.570C>T
  hgvsp: ENST00000298877.1:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.274C>T
  hgvsp: ENST00000525557.1:c.274C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.621C>T
  hgvsp: ENST00000531433.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.621C>T
  hgvsp: ENST00000532405.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.74C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.429C>T
  hgvsp: ENST00000393265.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16571
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6663
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser207Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

14-92909783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909783
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909783
    reference: chr 14
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.571G>A
  hgvsp: ENSP00000337789.5:p.Val191Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.622G>A
  hgvsp: ENSP00000431840.1:p.Val208Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.275G>A
  hgvsp: ENSP00000432464.1:p.Val93Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.430G>A
  hgvsp: ENSP00000376948.2:p.Val144Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.622G>A
  hgvsp: ENSP00000433302.1:p.Val208Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.571G>A
  hgvsp: ENSP00000298877.1:p.Val191Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.75G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val208Met
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

14-92909797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909797
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909797
    reference: chr 14
allele count: 1
allele frequency: 8.271572260455268e-6
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.289C>T
  hgvsp: ENST00000525557.1:c.289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.444C>T
  hgvsp: ENST00000393265.2:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.636C>T
  hgvsp: ENST00000531433.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.89C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.636C>T
  hgvsp: ENST00000532405.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.585C>T
  hgvsp: ENST00000351924.5:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.585C>T
  hgvsp: ENST00000298877.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2881
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6663
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile212Ile
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

14-92909804-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909804
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909804
    reference: chr 14
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.643A>G
  hgvsp: ENSP00000433302.1:p.Ile215Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.296A>G
  hgvsp: ENSP00000432464.1:p.Ile100Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.643A>G
  hgvsp: ENSP00000431840.1:p.Ile215Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.96A>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.592A>G
  hgvsp: ENSP00000337789.5:p.Ile198Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.451A>G
  hgvsp: ENSP00000376948.2:p.Ile151Val
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.592A>G
  hgvsp: ENSP00000298877.1:p.Ile198Val
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6749
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile215Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

14-92909806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909806
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909806
    reference: chr 14
allele count: 2
allele frequency: 1.655519502019734e-5
allele num: 120808
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.645C>T
  hgvsp: ENST00000532405.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.298C>T
  hgvsp: ENST00000525557.1:c.298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.594C>T
  hgvsp: ENST00000351924.5:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.645C>T
  hgvsp: ENST00000531433.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.594C>T
  hgvsp: ENST00000298877.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.98C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.453C>T
  hgvsp: ENST00000393265.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36816
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6744
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile215Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-92909808-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909808
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909808
    reference: chr 14
allele count: 3
allele frequency: 2.483197033407277e-5
allele num: 120812
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.300T>C
  hgvsp: ENSP00000432464.1:p.Val101Ala
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.100T>C
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.596T>C
  hgvsp: ENSP00000298877.1:p.Val199Ala
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.596T>C
  hgvsp: ENSP00000337789.5:p.Val199Ala
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.647T>C
  hgvsp: ENSP00000433302.1:p.Val216Ala
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.455T>C
  hgvsp: ENSP00000376948.2:p.Val152Ala
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.647T>C
  hgvsp: ENSP00000431840.1:p.Val216Ala
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16683
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6665
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val216Ala
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

14-92909811-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909811
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909811
    reference: chr 14
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.650T>A
  hgvsp: ENSP00000431840.1:p.Leu217His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.303T>A
  hgvsp: ENSP00000432464.1:p.Leu102His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.599T>A
  hgvsp: ENSP00000337789.5:p.Leu200His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.103T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.458T>A
  hgvsp: ENSP00000376948.2:p.Leu153His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.650T>A
  hgvsp: ENSP00000433302.1:p.Leu217His
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.599T>A
  hgvsp: ENSP00000298877.1:p.Leu200His
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2878
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu217His
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-92909815-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909815
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909815
    reference: chr 14
allele count: 3
allele frequency: 2.484842460987973e-5
allele num: 120732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.307C>T
  hgvsp: ENST00000525557.1:c.307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.654C>T
  hgvsp: ENST00000531433.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.603C>T
  hgvsp: ENST00000298877.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.107C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.603C>T
  hgvsp: ENST00000351924.5:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.654C>T
  hgvsp: ENST00000532405.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.462C>T
  hgvsp: ENST00000393265.2:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile218Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

14-92909816-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909816
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909816
    reference: chr 14
allele count: 98
allele frequency: 8.119573142440512e-4
allele num: 120696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.463G>A
  hgvsp: ENSP00000376948.2:p.Val155Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.308G>A
  hgvsp: ENSP00000432464.1:p.Val104Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.108G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.655G>A
  hgvsp: ENSP00000431840.1:p.Val219Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.655G>A
  hgvsp: ENSP00000433302.1:p.Val219Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.604G>A
  hgvsp: ENSP00000337789.5:p.Val202Met
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.604G>A
  hgvsp: ENSP00000298877.1:p.Val202Met
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val219Met
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

14-92909818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909818
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909818
    reference: chr 14
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465G>A
  hgvsp: ENST00000393265.2:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606G>A
  hgvsp: ENST00000351924.5:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657G>A
  hgvsp: ENST00000531433.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606G>A
  hgvsp: ENST00000298877.1:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657G>A
  hgvsp: ENST00000532405.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310G>A
  hgvsp: ENST00000525557.1:c.310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 2.25e1
  variant carriers: 0
hgvs: c.657G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

14-92909832-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909832
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909832
    reference: chr 14
allele count: 101
allele frequency: 8.391910530601393e-4
allele num: 120354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+14C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+14C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 24781
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16457
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35344
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6551
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

14-92909833-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909833
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909833
    reference: chr 14
allele count: 1
allele frequency: 8.311308366163002e-6
allele num: 120318
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+15T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+15T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+15T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+15T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+15T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+15T>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+15T>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-92909834-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909834
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909834
    reference: chr 14
allele count: 1
allele frequency: 8.315870006320061e-6
allele num: 120252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+16G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+16G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+16G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+16G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+16G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+16G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+16G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16357
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-92909835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909835
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909835
    reference: chr 14
allele count: 1
allele frequency: 8.321129010784183e-6
allele num: 120176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+17C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+17C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6658
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

14-92909838-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909838
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909838
    reference: chr 14
allele count: 8
allele frequency: 6.66045024643666e-5
allele num: 120112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+20C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+20C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+20C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+20C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+20C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+20C>G
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+20C>G
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16400
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6666
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 6449
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

14-92909838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909838
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909838
    reference: chr 14
allele count: 1
allele frequency: 8.325562808045825e-6
allele num: 120112
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+20C>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+20C>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

14-92909840-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909840
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909840
    reference: chr 14
allele count: 1
allele frequency: 8.330278897737497e-6
allele num: 120044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+22A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+22A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+22A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+22A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+22A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+22A>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+22A>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16289
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6659
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-92909842-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909842
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909842
    reference: chr 14
allele count: 1
allele frequency: 8.340561820244212e-6
allele num: 119896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+24G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+24G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+24G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+24G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+24G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+24G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+24G>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15881
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31900
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

14-92909847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909847
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909847
    reference: chr 14
allele count: 1
allele frequency: 8.351009637065121e-6
allele num: 119746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+29G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+29G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+29G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+29G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+29G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+29G>A
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+29G>A
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20283
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6658
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

14-92909852-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 92909852
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 92909852
    reference: chr 14
allele count: 131
allele frequency: 1.095317725752508e-3
allele num: 119600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000337789
  ensembl transcript: ENST00000351924
  gene symbol: SLC24A4
  hgvsc: ENST00000351924.5:c.606+34G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000298877
  ensembl transcript: ENST00000298877
  gene symbol: SLC24A4
  hgvsc: ENST00000298877.1:c.606+34G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000433302
  ensembl transcript: ENST00000531433
  gene symbol: SLC24A4
  hgvsc: ENST00000531433.1:c.657+34G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl transcript: ENST00000554925
  gene symbol: SLC24A4
  hgvsc: ENST00000554925.1:n.110+34G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000431840
  ensembl transcript: ENST00000532405
  gene symbol: SLC24A4
  hgvsc: ENST00000532405.1:c.657+34G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000432464
  ensembl transcript: ENST00000525557
  gene symbol: SLC24A4
  hgvsc: ENST00000525557.1:c.310+34G>T
  variant of: http://identifiers.org/hgnc/10978
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140090
  ensembl protein: ENSP00000376948
  ensembl transcript: ENST00000393265
  gene symbol: SLC24A4
  hgvsc: ENST00000393265.2:c.465+34G>T
  variant of: http://identifiers.org/hgnc/10978
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18529
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14685
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 2
reference allele: G

GenotypeQuality
all individuals: 2507
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11645
bin: 9.75e1
variant carriers: 9

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.239854633555421e-4
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.418155e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.02e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4794
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11645
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3764
bin: 8.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.183e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.41e-1

DP
type: SiteQuality
SIO_000300: 2.418155e6

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4793
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11635
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3409
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3765
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49288176232579e-5
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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

QD
type: SiteQuality
SIO_000300: 1.199e1

FS
type: SiteQuality
SIO_000300: 6.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.55e0

VQSLOD
type: SiteQuality
SIO_000300: 8.129999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.417846e6

GenotypeQuality
all individuals: 11611
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8911
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4795
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.344e0

FS
type: SiteQuality
SIO_000300: 7.288e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.087e0

MQRankSum
type: SiteQuality
SIO_000300: -1.05e0

QD
type: SiteQuality
SIO_000300: 8.74e0

DP
type: SiteQuality
SIO_000300: 2.417271e6

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11606
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24014
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495863805299125e-5
allele num: 66728
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.932e1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 2.417242e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 9.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.89e-1

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4797
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994664748373947e-5
allele num: 66726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.116e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.417053e6

VQSLOD
type: SiteQuality
SIO_000300: 7.5e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

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

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

GenotypeQuality
all individuals: 11594
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8910
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.238e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.416589e6

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

QD
type: SiteQuality
SIO_000300: 1.093e1

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1669
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.012e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.332e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.416532e6

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

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

GenotypeQuality
all individuals: 8906
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3758
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11592
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4791
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

VQSLOD
type: SiteQuality
SIO_000300: -1.485e0

FS
type: SiteQuality
SIO_000300: 6.738e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.299e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.341e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.085e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 2.416304e6

GenotypeQuality
all individuals: 4787
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3756
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11590
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2500
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3402
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
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

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 2.416158e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.14e-1

FS
type: SiteQuality
SIO_000300: 3.188e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.75e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.063e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.662e0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8890
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.635922918434129e-4
allele num: 16502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 464
allele frequency: 4.458965981164713e-2
allele num: 10406
num of homozygotes: 9

Latino
type: Population
allele count: 27
allele frequency: 2.333218112685793e-3
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.995771987166032e-5
allele num: 66698
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 2.424535e6

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4812
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11254
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1670
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24198
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049569676432663e-4
allele num: 66694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.029385034837928e-4
allele num: 6602
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

DP
type: SiteQuality
SIO_000300: 2.389289e6

QD
type: SiteQuality
SIO_000300: 1.304e1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.73e-1

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

GenotypeQuality
all individuals: 24198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8943
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11254
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3764
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.304e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

FS
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 2.389289e6

GenotypeQuality
all individuals: 3747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8878
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11221
bin: 9.75e1
variant carriers: 16

African
type: Population
allele count: 16
allele frequency: 1.5381657373582e-3
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

DP
type: SiteQuality
SIO_000300: 2.381731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.505e0

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23983
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8878
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11221
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.505e0

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

DP
type: SiteQuality
SIO_000300: 2.381731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22933
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003544182134919e-5
allele num: 66588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.403e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 2.361601e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -8.734e-1

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3679
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007971123477215e-5
allele num: 66490
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 2.338122e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.455e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11146
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 8339
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22065
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.852822192255828e-4
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.455e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

DP
type: SiteQuality
SIO_000300: 2.338122e6

GenotypeQuality
all individuals: 530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3656
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11136
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4574
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.334575e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
type: SiteQuality
SIO_000300: -4.05e-1

GenotypeQuality
all individuals: 2422
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8146
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504211793020457e-5
allele num: 66480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.021e0

FS
type: SiteQuality
SIO_000300: 3.245e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

QD
type: SiteQuality
SIO_000300: 1.476e1

MQ
type: SiteQuality
SIO_000300: 5.884e1

DP
type: SiteQuality
SIO_000300: 2.325806e6

GenotypeQuality
all individuals: 2376
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6392
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11061
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13998
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

Latino
type: Population
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
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508432135638218e-5
allele num: 66294
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.073e0

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 2.218896e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-1

GenotypeQuality
all individuals: 12161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2636
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2730
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11058
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509980974239725e-5
allele num: 66226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
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
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16004
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.208467e6

MQ
type: SiteQuality
SIO_000300: 5.907e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.182e0

FS
type: SiteQuality
SIO_000300: 6.576e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.874e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.45e-1

GenotypeQuality
all individuals: 96
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.271951831409934e-5
allele num: 15944
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.088e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 2.198089e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.326e1

GenotypeQuality
all individuals: 2371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2162
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4076
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15890
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027550711474417e-5
allele num: 66060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.565e0

DP
type: SiteQuality
SIO_000300: 2.196547e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.94e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

GenotypeQuality
all individuals: 3543
bin: 3.75e1
variant carriers: 52

GenotypeQuality
all individuals: 1756
bin: 2.75e1
variant carriers: 31

GenotypeQuality
all individuals: 1725
bin: 7.25e1
variant carriers: 41

GenotypeQuality
all individuals: 762
bin: 5.75e1
variant carriers: 47

GenotypeQuality
all individuals: 1057
bin: 9.25e1
variant carriers: 80

GenotypeQuality
all individuals: 2946
bin: 2.25e1
variant carriers: 25

GenotypeQuality
all individuals: 747
bin: 8.75e1
variant carriers: 57

South Asian
type: Population
allele count: 1909
allele frequency: 1.215304303539598e-1
allele num: 15708
num of homozygotes: 112

East Asian
type: Population
allele count: 1510
allele frequency: 1.842811813522089e-1
allele num: 8194
num of homozygotes: 146

African
type: Population
allele count: 2802
allele frequency: 2.818913480885312e-1
allele num: 9940
num of homozygotes: 385

European (Finnish)
type: Population
allele count: 184
allele frequency: 3.286888174347982e-2
allele num: 5598
num of homozygotes: 4

Other
type: Population
allele count: 83
allele frequency: 9.952038369304557e-2
allele num: 834
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 2389
allele frequency: 3.753220637214856e-2
allele num: 63652
num of homozygotes: 52

Latino
type: Population
allele count: 1666
allele frequency: 1.556427503736921e-1
allele num: 10704
num of homozygotes: 129

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 1.589078e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.736e1

GenotypeQuality
all individuals: 3195
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3716
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10934
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.998000399920016e-5
allele num: 10002
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.345982992765579e-5
allele num: 15758
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.201056930098487e-4
allele num: 8326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63968
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.099e0

DP
type: SiteQuality
SIO_000300: 1.594966e6

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.765e-1

FS
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 1.249e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: -5.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 2134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5629
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.978048293753742e-5
allele num: 10022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.345982992765579e-5
allele num: 15758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.685011087859575e-5
allele num: 64034
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.643177e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.005e0

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

GenotypeQuality
all individuals: 557
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 1028
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1281
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variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 1

GenotypeQuality
all individuals: 1992
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variant carriers: 2

GenotypeQuality
all individuals: 936
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 3
allele frequency: 3.537735849056604e-3
allele num: 848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 8.246716873093919e-4
allele num: 64268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.1936022917164e-4
allele num: 8378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 36
allele frequency: 6.331340133661625e-3
allele num: 5686
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 1.65389e6

QD
type: SiteQuality
SIO_000300: 1.375e1

GenotypeQuality
all individuals: 2030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6331
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variant carriers: 0

GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 32858
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variant carriers: 0

GenotypeQuality
all individuals: 2847
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GenotypeQuality
all individuals: 679
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variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.06654400490647e-5
allele num: 65220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

QD
type: SiteQuality
SIO_000300: 1.732e1

FS
type: SiteQuality
SIO_000300: 4.61e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

DP
type: SiteQuality
SIO_000300: 1.718074e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

GenotypeQuality
all individuals: 269
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
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variant carriers: 0

GenotypeQuality
all individuals: 653
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GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 2017
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variant carriers: 0

GenotypeQuality
all individuals: 6653
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 265
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.872892995380197e-4
allele num: 16018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.244e0

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.68e-1

DP
type: SiteQuality
SIO_000300: 1.721767e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 8.081e0

QD
type: SiteQuality
SIO_000300: 1.345e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6653
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 792
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 33673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6391
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.060162800660995e-5
allele num: 65356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 1.591e0

MQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.728656e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 1.152e1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2849
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.583231483744805e-5
allele num: 65456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.770851779706039e-4
allele num: 11294
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.734776e6

FS
type: SiteQuality
SIO_000300: 5.516e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.638e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
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variant carriers: 0

GenotypeQuality
all individuals: 6400
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variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 2.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2839
bin: 7.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.099045493987852e-4
allele num: 16134
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.951934970842905e-4
allele num: 11318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.631257631257631e-5
allele num: 65520
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.157407407407407e-3
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 275
allele frequency: 2.693437806072478e-2
allele num: 10210
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.745534e6

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.405e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

GenotypeQuality
all individuals: 1569
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
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GenotypeQuality
all individuals: 6504
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variant carriers: 0

GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 239
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 2857
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variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524111443028714e-5
allele num: 65612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.744948e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

FS
type: SiteQuality
SIO_000300: 1.668e0

QD
type: SiteQuality
SIO_000300: 9.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2858
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 1305
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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: 1300
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variant carriers: 0

GenotypeQuality
all individuals: 6664
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.773469029654326e-5
allele num: 11398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.85e-1

DP
type: SiteQuality
SIO_000300: 1.754246e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.677e0

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.441e1

GenotypeQuality
all individuals: 2040
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 314
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variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.669e1

VQSLOD
type: SiteQuality
SIO_000300: -2.541e0

FS
type: SiteQuality
SIO_000300: 1.309e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 1.759093e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.863e0

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1302
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variant carriers: 0

GenotypeQuality
all individuals: 6555
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.755034144633164e-5
allele num: 11422
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65932
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.760384e6

QD
type: SiteQuality
SIO_000300: 8.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.298e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

FS
type: SiteQuality
SIO_000300: 3.069e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

GenotypeQuality
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bin: 8.25e1
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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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1279
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GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.811616954474098e-5
allele num: 10192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.684068710003368e-4
allele num: 5938
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.065384147083891e-4
allele num: 65704
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.02313e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.654e0

MQ
type: SiteQuality
SIO_000300: 5.865e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.771088e6

QD
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.546e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: -5.115e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

GenotypeQuality
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bin: 6.25e1
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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GenotypeQuality
all individuals: 937
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GenotypeQuality
all individuals: 2031
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509889778046203e-5
allele num: 66230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.587e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 1.771434e6

QD
type: SiteQuality
SIO_000300: 1.418e1

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

GenotypeQuality
all individuals: 2031
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 118
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GenotypeQuality
all individuals: 6664
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 937
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.059338668277215e-5
allele num: 66230
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

FS
type: SiteQuality
SIO_000300: 2.587e0

DP
type: SiteQuality
SIO_000300: 1.771434e6

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.418e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
all individuals: 724
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2033
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50952510340247e-5
allele num: 66246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

FS
type: SiteQuality
SIO_000300: 1.194e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.088e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

DP
type: SiteQuality
SIO_000300: 1.772434e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.32e-1

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.32e-1

FS
type: SiteQuality
SIO_000300: 1.194e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

QD
type: SiteQuality
SIO_000300: 1.088e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

DP
type: SiteQuality
SIO_000300: 1.772434e6

GenotypeQuality
all individuals: 6700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6670
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variant carriers: 12

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: 77
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variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.659876263769428e-4
allele num: 66270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.248e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

DP
type: SiteQuality
SIO_000300: 1.773105e6

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.184e0

GenotypeQuality
all individuals: 6663
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 36282
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 161
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.740947075208914e-4
allele num: 11488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 9.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

DP
type: SiteQuality
SIO_000300: 1.776196e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 6663
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 157
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GenotypeQuality
all individuals: 2034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
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variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.216397031991242e-4
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013409673045051e-5
allele num: 66370
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.058e1

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

DP
type: SiteQuality
SIO_000300: 1.77707e6

GenotypeQuality
all individuals: 2033
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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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: 1

GenotypeQuality
all individuals: 938
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
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: 16448
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.019e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 6.304e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e-1

DP
type: SiteQuality
SIO_000300: 1.77837e6

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.25e1
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GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215362177929023e-4
allele num: 16456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.439e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.306e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.780175e6

QD
type: SiteQuality
SIO_000300: 1.161e1

FS
type: SiteQuality
SIO_000300: 4.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

VQSLOD
type: SiteQuality
SIO_000300: -1.558e-1

GenotypeQuality
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bin: 8.25e1
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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GenotypeQuality
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GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513857542655954e-5
allele num: 66462
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 9.56e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.217e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

DP
type: SiteQuality
SIO_000300: 1.781415e6

GenotypeQuality
all individuals: 40
bin: 4.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 434
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GenotypeQuality
all individuals: 6782
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GenotypeQuality
all individuals: 1292
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GenotypeQuality
all individuals: 6661
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.96e1

ClippingRankSum
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SIO_000300: -3.67e-1

DP
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SIO_000300: 1.782226e6

FS
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MQRankSum
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SIO_000300: -1.2e-2

ReadPosRankSum
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SIO_000300: 4.02e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.007157033740302e-5
allele num: 66508
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10360
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: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
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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MQ
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InbreedingCoeff
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QD
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MQRankSum
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DP
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FS
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ClippingRankSum
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SIO_000300: -3.24e-1

BaseQRankSum
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SIO_000300: 4.99e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

South Asian
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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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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
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African
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allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.784407e6

MQ
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SIO_000300: 6.0e1

VQSLOD
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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SIO_000300: 4.99e0

MQRankSum
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SIO_000300: 1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8634
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

Other
type: Population
allele count: 0
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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FS
type: SiteQuality
SIO_000300: 6.582e0

MQRankSum
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DP
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.918e0

VQSLOD
type: SiteQuality
SIO_000300: 9.4e-2

QD
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SIO_000300: 1.151e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
allele num: 10368
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: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

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

ReadPosRankSum
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SIO_000300: 2.19e0

InbreedingCoeff
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.233e0

FS
type: SiteQuality
SIO_000300: 1.607e0

DP
type: SiteQuality
SIO_000300: 1.786073e6

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
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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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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QD
type: SiteQuality
SIO_000300: 1.06e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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FS
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ClippingRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 898
num of homozygotes: 0

African
type: Population
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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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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MQ
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66504
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African
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Latino
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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 frequency: 0.0e0
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East Asian
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MQ
type: SiteQuality
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.007518796992481e-5
allele num: 66500
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South Asian
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Latino
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European (Finnish)
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East Asian
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African
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Other
type: Population
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QD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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FS
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VQSLOD
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10370
num of homozygotes: 0

South Asian
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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: 3.475440222428174e-4
allele num: 8632
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European (Non-Finnish)
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European (Finnish)
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Other
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MQRankSum
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.676e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.61e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.68e-1

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: -9.212e-1

DP
type: SiteQuality
SIO_000300: 1.783343e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.357e1

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.782003e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 3
allele frequency: 3.348214285714286e-3
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.074279763970844e-4
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 87
allele frequency: 8.399304885112957e-3
allele num: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

DP
type: SiteQuality
SIO_000300: 1.786496e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.113e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
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: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e0

DP
type: SiteQuality
SIO_000300: 1.7813e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

QD
type: SiteQuality
SIO_000300: 1.328e1

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 2.716e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.228e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 99

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

South Asian
type: Population
allele count: 1
allele frequency: 6.105751618024179e-5
allele num: 16378
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.610966057441253e-4
allele num: 11490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

African
type: Population
allele count: 95
allele frequency: 9.19295529320689e-3
allele num: 10334
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017683626048645e-5
allele num: 66276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

DP
type: SiteQuality
SIO_000300: 1.771907e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.36e-2

FS
type: SiteQuality
SIO_000300: 6.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 1.409e1

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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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

MQ
type: SiteQuality
SIO_000300: 5.882e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.948e-1

FS
type: SiteQuality
SIO_000300: 7.16e-1

DP
type: SiteQuality
SIO_000300: 1.766364e6

QD
type: SiteQuality
SIO_000300: 1.49e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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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GenotypeQuality
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variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11484
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-1

DP
type: SiteQuality
SIO_000300: 1.764417e6

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.191e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.01e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

African
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: 8600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510482750286992e-5
allele num: 66204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8
allele frequency: 6.977149834292691e-4
allele num: 11466
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 892
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6336
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

East Asian
type: Population
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South Asian
type: Population
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.756982e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.122199093914534e-5
allele num: 16334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.481e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.756982e6

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33598
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447535e-5
allele num: 66140
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.881e0

FS
type: SiteQuality
SIO_000300: 2.764e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.886e0

QD
type: SiteQuality
SIO_000300: 1.106e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.38e-1

DP
type: SiteQuality
SIO_000300: 1.750639e6

GenotypeQuality
all individuals: 6658
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 932
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2268
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.13421666053245e-5
allele num: 16302
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: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.179e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.487e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 1.737253e6

FS
type: SiteQuality
SIO_000300: 6.466e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

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

GenotypeQuality
all individuals: 2759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.759635599159075e-5
allele num: 11416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.576e1

DP
type: SiteQuality
SIO_000300: 1.717482e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.453e0

VQSLOD
type: SiteQuality
SIO_000300: -3.634e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.497e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 925
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2092
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6770
bin: 9.75e1
variant carriers: 129

GenotypeQuality
all individuals: 504
bin: 4.75e1
variant carriers: 0