9-130166200-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166200
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166200
    reference: chr 9
allele count: 1
allele frequency: 8.807003329047259e-6
allele num: 113546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-38C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-38C>G
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4538
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130166207-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166207
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166207
    reference: chr 9
allele count: 1
allele frequency: 8.772391529378739e-6
allele num: 113994
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-31A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-31A>G
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/9-130166208-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166208
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166208
    reference: chr 9
allele count: 1
allele frequency: 8.769314414999035e-6
allele num: 114034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-30C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-30C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4653
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

9-130166208-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166208
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166208
    reference: chr 9
allele count: 1
allele frequency: 8.769314414999035e-6
allele num: 114034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-30C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-30C>G
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28954
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

9-130166208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166208
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166208
    reference: chr 9
allele count: 1
allele frequency: 8.769314414999035e-6
allele num: 114034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-30C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-30C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4964
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3829
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-130166211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166211
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166211
    reference: chr 9
allele count: 1
allele frequency: 8.75196919306844e-6
allele num: 114260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-27G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-27G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5042
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

9-130166222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166222
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166222
    reference: chr 9
allele count: 1
allele frequency: 8.671673112610347e-6
allele num: 115318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-16G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-16G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16647
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

9-130166223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166223
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166223
    reference: chr 9
allele count: 6
allele frequency: 5.19777535214928e-5
allele num: 115434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-15C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-15C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16804
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2258
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/9-130166235-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166235
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166235
    reference: chr 9
allele count: 2
allele frequency: 1.712798026856673e-5
allele num: 116768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.79-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.385-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.385-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.868-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.379-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.868-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.527-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.463-3C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.661-3C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18424
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
hgvs: c.868-3C>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/9-130166251-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166251
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166251
    reference: chr 9
allele count: 1
allele frequency: 8.469982382436644e-6
allele num: 118064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.674C>A
  hgvsp: ENSP00000411726.1:p.Ala225Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.881C>A
  hgvsp: ENSP00000362458.3:p.Ala294Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.398C>A
  hgvsp: ENSP00000404893.1:p.Ala133Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.476C>A
  hgvsp: ENSP00000389070.1:p.Ala159Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.398C>A
  hgvsp: ENSP00000391213.1:p.Ala133Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.540C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.392C>A
  hgvsp: ENSP00000392434.1:p.Ala131Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.92C>A
  hgvsp: ENSP00000362450.1:p.Ala31Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.881C>A
  hgvsp: ENSP00000362469.3:p.Ala294Asp
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala294Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

9-130166254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166254
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166254
    reference: chr 9
allele count: 2
allele frequency: 1.691188905800778e-5
allele num: 118260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.95C>T
  hgvsp: ENSP00000362450.1:p.Ser32Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.543C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.884C>T
  hgvsp: ENSP00000362458.3:p.Ser295Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.677C>T
  hgvsp: ENSP00000411726.1:p.Ser226Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.401C>T
  hgvsp: ENSP00000404893.1:p.Ser134Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.401C>T
  hgvsp: ENSP00000391213.1:p.Ser134Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.884C>T
  hgvsp: ENSP00000362469.3:p.Ser295Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.479C>T
  hgvsp: ENSP00000389070.1:p.Ser160Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.395C>T
  hgvsp: ENSP00000392434.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser295Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

9-130166255-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166255
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166255
    reference: chr 9
allele count: 2
allele frequency: 1.690245592684617e-5
allele num: 118326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.396G>A
  hgvsp: ENST00000451404.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.96G>A
  hgvsp: ENST00000373352.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.544G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.480G>A
  hgvsp: ENST00000423934.1:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.402G>A
  hgvsp: ENST00000439597.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.678G>A
  hgvsp: ENST00000419917.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.402G>A
  hgvsp: ENST00000430147.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.885G>A
  hgvsp: ENST00000373360.3:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.885G>A
  hgvsp: ENST00000373371.3:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20477
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6136
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser295Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

9-130166259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166259
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166259
    reference: chr 9
allele count: 9
allele frequency: 7.591733445803459e-5
allele num: 118550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.406G>A
  hgvsp: ENSP00000391213.1:p.Val136Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.682G>A
  hgvsp: ENSP00000411726.1:p.Val228Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.400G>A
  hgvsp: ENSP00000392434.1:p.Val134Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.406G>A
  hgvsp: ENSP00000404893.1:p.Val136Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.100G>A
  hgvsp: ENSP00000362450.1:p.Val34Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.548G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.484G>A
  hgvsp: ENSP00000389070.1:p.Val162Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.889G>A
  hgvsp: ENSP00000362469.3:p.Val297Ile
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.889G>A
  hgvsp: ENSP00000362458.3:p.Val297Ile
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28596
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val297Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

9-130166261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166261
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166261
    reference: chr 9
allele count: 2
allele frequency: 1.685658418178141e-5
allele num: 118648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.891C>T
  hgvsp: ENST00000373360.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.486C>T
  hgvsp: ENST00000423934.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.408C>T
  hgvsp: ENST00000430147.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.102C>T
  hgvsp: ENST00000373352.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.408C>T
  hgvsp: ENST00000439597.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.891C>T
  hgvsp: ENST00000373371.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.684C>T
  hgvsp: ENST00000419917.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.550C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.402C>T
  hgvsp: ENST00000451404.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28734
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val297Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

9-130166262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166262
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166262
    reference: chr 9
allele count: 9
allele frequency: 7.581373407911584e-5
allele num: 118712
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.892G>A
  hgvsp: ENSP00000362469.3:p.Val298Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.685G>A
  hgvsp: ENSP00000411726.1:p.Val229Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.487G>A
  hgvsp: ENSP00000389070.1:p.Val163Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.409G>A
  hgvsp: ENSP00000391213.1:p.Val137Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.551G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.892G>A
  hgvsp: ENSP00000362458.3:p.Val298Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.403G>A
  hgvsp: ENSP00000392434.1:p.Val135Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.103G>A
  hgvsp: ENSP00000362450.1:p.Val35Met
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.409G>A
  hgvsp: ENSP00000404893.1:p.Val137Met
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6269
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val298Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

9-130166265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166265
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166265
    reference: chr 9
allele count: 1
allele frequency: 8.419776370739593e-6
allele num: 118768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.554G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.688G>A
  hgvsp: ENSP00000411726.1:p.Gly230Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.412G>A
  hgvsp: ENSP00000404893.1:p.Gly138Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.106G>A
  hgvsp: ENSP00000362450.1:p.Gly36Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.895G>A
  hgvsp: ENSP00000362458.3:p.Gly299Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.490G>A
  hgvsp: ENSP00000389070.1:p.Gly164Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.412G>A
  hgvsp: ENSP00000391213.1:p.Gly138Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.895G>A
  hgvsp: ENSP00000362469.3:p.Gly299Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.406G>A
  hgvsp: ENSP00000392434.1:p.Gly136Ser
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28846
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly299Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

9-130166266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166266
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166266
    reference: chr 9
allele count: 1
allele frequency: 8.418925745074929e-6
allele num: 118780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.896G>A
  hgvsp: ENSP00000362458.3:p.Gly299Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.689G>A
  hgvsp: ENSP00000411726.1:p.Gly230Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.407G>A
  hgvsp: ENSP00000392434.1:p.Gly136Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.896G>A
  hgvsp: ENSP00000362469.3:p.Gly299Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.413G>A
  hgvsp: ENSP00000404893.1:p.Gly138Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.413G>A
  hgvsp: ENSP00000391213.1:p.Gly138Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.107G>A
  hgvsp: ENSP00000362450.1:p.Gly36Asp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.555G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.491G>A
  hgvsp: ENSP00000389070.1:p.Gly164Asp
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly299Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130166278-T-TGTCCACA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166278
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166285
    reference: chr 9
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: TGTCCACA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.120_121insTCCACAG
  hgvsp: ENSP00000362450.1:p.Leu41SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.426_427insTCCACAG
  hgvsp: ENSP00000391213.1:p.Leu143SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.420_421insTCCACAG
  hgvsp: ENSP00000392434.1:p.Leu141SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.909_910insTCCACAG
  hgvsp: ENSP00000362458.3:p.Leu304SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.568_569insTCCACAG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.702_703insTCCACAG
  hgvsp: ENSP00000411726.1:p.Leu235SerfsTer?
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.909_910insTCCACAG
  hgvsp: ENSP00000362469.3:p.Leu304SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.504_505insTCCACAG
  hgvsp: ENSP00000389070.1:p.Leu169SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.426_427insTCCACAG
  hgvsp: ENSP00000404893.1:p.Leu143SerfsTer64
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21124
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu304SerfsTer64
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: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

9-130166295-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166295
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166294
    reference: chr 9
allele count: 9
allele frequency: 7.605976607396389e-5
allele num: 118328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.926delC
  hgvsp: ENSP00000362458.3:p.Ala309GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.585delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.137delC
  hgvsp: ENSP00000362450.1:p.Ala46GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.437delC
  hgvsp: ENSP00000392434.1:p.Ala146GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.443delC
  hgvsp: ENSP00000391213.1:p.Ala148GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.926delC
  hgvsp: ENSP00000362469.3:p.Ala309GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.719delC
  hgvsp: ENSP00000411726.1:p.Ala240GlyfsTer?
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.521delC
  hgvsp: ENSP00000389070.1:p.Ala174GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.443delC
  hgvsp: ENSP00000404893.1:p.Ala148GlyfsTer34
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20898
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala309GlyfsTer34
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: GC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

9-130166296-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166296
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166296
    reference: chr 9
allele count: 75
allele frequency: 6.343782247559759e-4
allele num: 118226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.719C>T
  hgvsp: ENSP00000411726.1:p.Ala240Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.137C>T
  hgvsp: ENSP00000362450.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.437C>T
  hgvsp: ENSP00000392434.1:p.Ala146Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.443C>T
  hgvsp: ENSP00000404893.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.926C>T
  hgvsp: ENSP00000362469.3:p.Ala309Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.585C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.926C>T
  hgvsp: ENSP00000362458.3:p.Ala309Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.521C>T
  hgvsp: ENSP00000389070.1:p.Ala174Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.443C>T
  hgvsp: ENSP00000391213.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20877
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 27948
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala309Val
num of homozygotes: 1
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

9-130166297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166297
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166297
    reference: chr 9
allele count: 7
allele frequency: 5.919861982646348e-5
allele num: 118246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.720G>A
  hgvsp: ENST00000419917.1:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.444G>A
  hgvsp: ENST00000430147.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.522G>A
  hgvsp: ENST00000423934.1:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.438G>A
  hgvsp: ENST00000451404.1:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.444G>A
  hgvsp: ENST00000439597.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.586G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.927G>A
  hgvsp: ENST00000373371.3:c.927G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.138G>A
  hgvsp: ENST00000373352.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.927G>A
  hgvsp: ENST00000373360.3:c.927G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28030
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala309Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

9-130166298-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166298
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166298
    reference: chr 9
allele count: 3
allele frequency: 2.53686916520092e-5
allele num: 118256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.587G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.445G>T
  hgvsp: ENSP00000404893.1:p.Ala149Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.439G>T
  hgvsp: ENSP00000392434.1:p.Ala147Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.139G>T
  hgvsp: ENSP00000362450.1:p.Ala47Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.445G>T
  hgvsp: ENSP00000391213.1:p.Ala149Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.928G>T
  hgvsp: ENSP00000362469.3:p.Ala310Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.523G>T
  hgvsp: ENSP00000389070.1:p.Ala175Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.721G>T
  hgvsp: ENSP00000411726.1:p.Ala241Ser
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.928G>T
  hgvsp: ENSP00000362458.3:p.Ala310Ser
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala310Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

9-130166307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166307
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166307
    reference: chr 9
allele count: 1
allele frequency: 8.483922965979469e-6
allele num: 117870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.596A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.937A>G
  hgvsp: ENSP00000362469.3:p.Met313Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.6A>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.454A>G
  hgvsp: ENSP00000391213.1:p.Met152Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.937A>G
  hgvsp: ENSP00000362458.3:p.Met313Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.454A>G
  hgvsp: ENSP00000404893.1:p.Met152Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.730A>G
  hgvsp: ENSP00000411726.1:p.Met244Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.148A>G
  hgvsp: ENSP00000362450.1:p.Met50Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.532A>G
  hgvsp: ENSP00000389070.1:p.Met178Val
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.448A>G
  hgvsp: ENSP00000392434.1:p.Met150Val
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met313Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

9-130166307-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166307
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166307
    reference: chr 9
allele count: 1
allele frequency: 8.483922965979469e-6
allele num: 117870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.532A>T
  hgvsp: ENSP00000389070.1:p.Met178Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.454A>T
  hgvsp: ENSP00000391213.1:p.Met152Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.454A>T
  hgvsp: ENSP00000404893.1:p.Met152Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.448A>T
  hgvsp: ENSP00000392434.1:p.Met150Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.937A>T
  hgvsp: ENSP00000362458.3:p.Met313Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.730A>T
  hgvsp: ENSP00000411726.1:p.Met244Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.596A>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.148A>T
  hgvsp: ENSP00000362450.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.6A>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.937A>T
  hgvsp: ENSP00000362469.3:p.Met313Leu
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Met313Leu
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: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-130166322-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166322
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166322
    reference: chr 9
allele count: 1
allele frequency: 8.66145824310981e-6
allele num: 115454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.463C>A
  hgvsp: ENST00000451404.1:c.463C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.547C>A
  hgvsp: ENST00000423934.1:c.547C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.952C>A
  hgvsp: ENST00000373360.3:c.952C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.952C>A
  hgvsp: ENST00000373371.3:c.952C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.611C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.469C>A
  hgvsp: ENST00000430147.1:c.469C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.469C>A
  hgvsp: ENST00000439597.1:c.469C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.745C>A
  hgvsp: ENST00000419917.1:c.745C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.21C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.163C>A
  hgvsp: ENST00000373352.1:c.163C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg318Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

9-130166322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166322
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166322
    reference: chr 9
allele count: 8
allele frequency: 6.929166594487848e-5
allele num: 115454
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.952C>T
  hgvsp: ENSP00000362469.3:p.Arg318Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.463C>T
  hgvsp: ENSP00000392434.1:p.Arg155Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.952C>T
  hgvsp: ENSP00000362458.3:p.Arg318Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.469C>T
  hgvsp: ENSP00000391213.1:p.Arg157Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.611C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.469C>T
  hgvsp: ENSP00000404893.1:p.Arg157Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.21C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.745C>T
  hgvsp: ENSP00000411726.1:p.Arg249Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.163C>T
  hgvsp: ENSP00000362450.1:p.Arg55Trp
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.547C>T
  hgvsp: ENSP00000389070.1:p.Arg183Trp
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24503
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19923
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg318Trp
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

9-130166323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166323
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166323
    reference: chr 9
allele count: 3
allele frequency: 2.596773076656741e-5
allele num: 115528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.953G>A
  hgvsp: ENSP00000362458.3:p.Arg318Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.470G>A
  hgvsp: ENSP00000391213.1:p.Arg157Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.464G>A
  hgvsp: ENSP00000392434.1:p.Arg155Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.22G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.548G>A
  hgvsp: ENSP00000389070.1:p.Arg183Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.612G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.746G>A
  hgvsp: ENSP00000411726.1:p.Arg249Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.470G>A
  hgvsp: ENSP00000404893.1:p.Arg157Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.953G>A
  hgvsp: ENSP00000362469.3:p.Arg318Gln
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.164G>A
  hgvsp: ENSP00000362450.1:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Arg318Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-130166327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166327
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166327
    reference: chr 9
allele count: 1
allele frequency: 8.77608691836484e-6
allele num: 113946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.474G>A
  hgvsp: ENST00000430147.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.957G>A
  hgvsp: ENST00000373360.3:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.26G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.552G>A
  hgvsp: ENST00000423934.1:c.552G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.750G>A
  hgvsp: ENST00000419917.1:c.750G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.957G>A
  hgvsp: ENST00000373371.3:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.468G>A
  hgvsp: ENST00000451404.1:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.168G>A
  hgvsp: ENST00000373352.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.474G>A
  hgvsp: ENST00000439597.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.616G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg319Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

9-130166335-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166335
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166335
    reference: chr 9
allele count: 1
allele frequency: 8.90805109658109e-6
allele num: 112258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.758T>C
  hgvsp: ENSP00000411726.1:p.Leu253Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.560T>C
  hgvsp: ENSP00000389070.1:p.Leu187Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.482T>C
  hgvsp: ENSP00000391213.1:p.Leu161Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.34T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.8T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.965T>C
  hgvsp: ENSP00000362469.3:p.Leu322Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.176T>C
  hgvsp: ENSP00000362450.1:p.Leu59Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.482T>C
  hgvsp: ENSP00000404893.1:p.Leu161Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.476T>C
  hgvsp: ENSP00000392434.1:p.Leu159Pro
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.624T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.965T>C
  hgvsp: ENSP00000362458.3:p.Leu322Pro
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu322Pro
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

9-130166342-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166342
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166342
    reference: chr 9
allele count: 1
allele frequency: 9.11244760342628e-6
allele num: 109740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.631G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.183G>T
  hgvsp: ENSP00000362450.1:p.Leu61Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.41G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.483G>T
  hgvsp: ENSP00000392434.1:p.Leu161Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.489G>T
  hgvsp: ENSP00000404893.1:p.Leu163Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.567G>T
  hgvsp: ENSP00000389070.1:p.Leu189Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.489G>T
  hgvsp: ENSP00000391213.1:p.Leu163Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.972G>T
  hgvsp: ENSP00000362469.3:p.Leu324Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.765G>T
  hgvsp: ENSP00000411726.1:p.Leu255Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.972G>T
  hgvsp: ENSP00000362458.3:p.Leu324Phe
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.15G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu324Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

9-130166343-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166343
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166343
    reference: chr 9
allele count: 1
allele frequency: 9.120592473687091e-6
allele num: 109642
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.632T>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.490T>G
  hgvsp: ENSP00000404893.1:p.Ser164Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.42T>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000411726
  ensembl transcript: ENST00000419917
  gene symbol: SLC2A8
  hgvsc: ENST00000419917.1:c.766T>G
  hgvsp: ENSP00000411726.1:p.Ser256Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.973T>G
  hgvsp: ENSP00000362458.3:p.Ser325Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.973T>G
  hgvsp: ENSP00000362469.3:p.Ser325Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.568T>G
  hgvsp: ENSP00000389070.1:p.Ser190Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.16T>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.490T>G
  hgvsp: ENSP00000391213.1:p.Ser164Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.184T>G
  hgvsp: ENSP00000362450.1:p.Ser62Ala
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.484T>G
  hgvsp: ENSP00000392434.1:p.Ser162Ala
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser325Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

9-130166352-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166352
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166352
    reference: chr 9
allele count: 3
allele frequency: 2.917323064356147e-5
allele num: 102834
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.25G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+6G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+6G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20483
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4981
  bin: 3.25e1
  variant carriers: 0
hgvs: c.976+6G>T
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

9-130166353-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166353
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166353
    reference: chr 9
allele count: 2
allele frequency: 2.098283604011918e-5
allele num: 95316
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+7G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.26G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+7G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6237
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19508
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
hgvs: c.976+7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-130166357-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166357
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166357
    reference: chr 9
allele count: 1089
allele frequency: 1.855954734474061e-2
allele num: 58676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.30A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+11A>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+11A>C
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 13915
  bin: 1.75e1
  variant carriers: 474
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 19122
  bin: 1.25e1
  variant carriers: 396
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 2.75e1
  variant carriers: 260
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 11439
  bin: 7.5e0
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.25e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 2.25e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 4.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 9.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 6.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 11224
  bin: 7.5e0
  variant carriers: 262
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

9-130166358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166358
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166358
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 87176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+12C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+12C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11362
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10658
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

9-130166359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166359
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166359
    reference: chr 9
allele count: 9
allele frequency: 1.168406293815236e-4
allele num: 77028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.32C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+13C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+13C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11797
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19496
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14592
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

9-130166361-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166361
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166360
    reference: chr 9
allele count: 1
allele frequency: 1.401345291479821e-5
allele num: 71360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.35delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+16delT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+16delT
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11028
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22476
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: CT
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS

9-130166365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166365
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166365
    reference: chr 9
allele count: 3
allele frequency: 5.206344798861546e-5
allele num: 57622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.38G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+19G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+19G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19305
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16842
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

9-130166365-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166365
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166365
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 57622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+19G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.38G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+19G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16842
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19305
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-130166366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166366
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166366
    reference: chr 9
allele count: 1
allele frequency: 2.074602713580349e-5
allele num: 48202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.39C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+20C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+20C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16033
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20102
  bin: 7.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 11978
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum

9-130166368-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166368
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166368
    reference: chr 9
allele count: 2
allele frequency: 5.104384666428462e-5
allele num: 39182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.41G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+22G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+22G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20710
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7119
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-130166369-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166369
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166369
    reference: chr 9
allele count: 1
allele frequency: 2.209261223047013e-5
allele num: 45264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.42C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+23C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+23C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15583
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20822
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10715
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/9-130166370-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166370
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166370
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 44324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.43C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+24C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+24C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21022
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18435
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

9-130166370-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166370
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166370
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 44324
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.43C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+24C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+24C>G
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21022
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4861
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

9-130166371-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166371
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166371
    reference: chr 9
allele count: 29
allele frequency: 8.140122382529613e-4
allele num: 35626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.44T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+25T>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+25T>C
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 1.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 21558
  bin: 7.5e0
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 7092
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

9-130166372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166372
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166372
    reference: chr 9
allele count: 2
allele frequency: 2.26510827217541e-5
allele num: 88296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.45C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+26C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+26C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21079
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5691
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/9-130166373-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166373
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166373
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 90234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.46C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+27C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+27C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21542
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

9-130166373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166373
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166373
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 90234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.46C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+27C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+27C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21542
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/9-130166374-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166374
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166374
    reference: chr 9
allele count: 2
allele frequency: 2.125488862438361e-5
allele num: 94096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.47C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+28C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+28C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21822
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 2.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8463
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

9-130166374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166374
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166374
    reference: chr 9
allele count: 1
allele frequency: 1.06274443121918e-5
allele num: 94096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.47C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+28C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+28C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21822
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6429
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

9-130166375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166375
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166375
    reference: chr 9
allele count: 2
allele frequency: 2.13024306073323e-5
allele num: 93886
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.48C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+29C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+29C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21573
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8364
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-130166375-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166375
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166375
    reference: chr 9
allele count: 2
allele frequency: 2.13024306073323e-5
allele num: 93886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.48C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+29C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+29C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10056
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21573
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8364
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

9-130166375-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166375
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166375
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 93886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.48C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+29C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+29C>G
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10056
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8364
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

9-130166376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166376
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166376
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 93534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.49G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+30G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+30G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21279
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8194
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 5.75e1
  variant carriers: 3
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

9-130166376-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166376
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166376
    reference: chr 9
allele count: 2
allele frequency: 2.138259884106314e-5
allele num: 93534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.49G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+30G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+30G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21279
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11858
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7175
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/9-130166377-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166377
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166377
    reference: chr 9
allele count: 1
allele frequency: 1.057015411284697e-5
allele num: 94606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.50C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+31C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+31C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21151
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8206
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5280
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

9-130166377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166377
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166377
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 94606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+31C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.50C>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+31C>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21151
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6244
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-130166378-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166378
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166378
    reference: chr 9
allele count: 19
allele frequency: 2.008074573548374e-4
allele num: 94618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.51C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+32C>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+32C>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21003
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11363
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18198
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 1.25e1
  variant carriers: 5
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

9-130166380-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166380
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166381
    reference: chr 9
allele count: 4
allele frequency: 4.227704145263915e-5
allele num: 94614
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.54dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+35dupG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+35dupG
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20694
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

9-130166380-TGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166380
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166378
    reference: chr 9
allele count: 1
allele frequency: 1.056926036315979e-5
allele num: 94614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+36_493+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+36_571+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+36_635+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+36_976+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+36_487+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.55_56delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+36_45+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+36_187+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+36_493+37delCG
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+36_976+37delCG
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10764
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5989
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5060
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7334
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: TGC
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

9-130166381-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166381
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166380
    reference: chr 9
allele count: 31
allele frequency: 3.316998009801194e-4
allele num: 93458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.55delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+36delC
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+36delC
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20482
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6975
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5034
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 6.75e1
  variant carriers: 1
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: GC
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

9-130166381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166381
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166381
    reference: chr 9
allele count: 2
allele frequency: 2.13999871600077e-5
allele num: 93458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.54G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+35G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+35G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

9-130166381-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166381
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166381
    reference: chr 9
allele count: 1
allele frequency: 1.069999358000385e-5
allele num: 93458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.54G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+35G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+35G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7855
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5034
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

9-130166382-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166382
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166382
    reference: chr 9
allele count: 96699
allele frequency: 9.45471078258829e-1
allele num: 102276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.55C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+36C>G
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+36C>G
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.5e0
  variant carriers: 1278
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 3.25e1
  variant carriers: 1915
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 861
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 16521
  bin: 1.75e1
  variant carriers: 16448
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 7.5e0
  variant carriers: 6006
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 2.75e1
  variant carriers: 4704
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 10239
  bin: 2.25e1
  variant carriers: 10204
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 320
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 15245
  bin: 1.25e1
  variant carriers: 15076
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 122
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 5.75e1
  variant carriers: 2640
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.5e0
  variant carriers: 157
genotype quality: GenotypeQuality
  all individuals: 4473
  bin: 6.25e1
  variant carriers: 4436
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 2.25e1
  variant carriers: 2426
num of homozygotes: 45770
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

9-130166383-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166383
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166383
    reference: chr 9
allele count: 9
allele frequency: 9.188361408882082e-5
allele num: 97950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.56G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+37G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+37G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18108
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14916
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3377
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

9-130166383-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166383
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166383
    reference: chr 9
allele count: 79
allele frequency: 8.065339458907606e-4
allele num: 97950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.56G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+37G>C
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+37G>C
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14916
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 18108
  bin: 1.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3377
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP

9-130166383-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166383
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166383
    reference: chr 9
allele count: 25174
allele frequency: 2.570086778968861e-1
allele num: 97950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.56G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+37G>T
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+37G>T
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 754
genotype depth: GenotypeDepth
  all individuals: 18108
  bin: 1.25e1
  variant carriers: 6449
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 347
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.5e0
  variant carriers: 499
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 7.5e0
  variant carriers: 2342
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 14916
  bin: 1.75e1
  variant carriers: 7088
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 2.75e1
  variant carriers: 1872
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.25e1
  variant carriers: 4151
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 80
genotype quality: GenotypeQuality
  all individuals: 8409
  bin: 2.25e1
  variant carriers: 404
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 5.75e1
  variant carriers: 273
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 1.75e1
  variant carriers: 333
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 566
num of homozygotes: 3817
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

9-130166384-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166384
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166386
    reference: chr 9
allele count: 1
allele frequency: 1.004540523164704e-5
allele num: 99548
alternate allele: GTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+38_45+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+38_487+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+38_976+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+38_187+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+38_635+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+38_493+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.57_58insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+38_976+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+38_493+39insTT
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+38_571+39insTT
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13220
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21040
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5723
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130166387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130166387
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130166387
    reference: chr 9
allele count: 3
allele frequency: 3.071315956510166e-5
allele num: 97678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362458
  ensembl transcript: ENST00000373360
  gene symbol: SLC2A8
  hgvsc: ENST00000373360.3:c.976+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000485806
  gene symbol: SLC2A8
  hgvsc: ENST00000485806.1:n.60G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000404893
  ensembl transcript: ENST00000439597
  gene symbol: SLC2A8
  hgvsc: ENST00000439597.1:c.493+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362469
  ensembl transcript: ENST00000373371
  gene symbol: SLC2A8
  hgvsc: ENST00000373371.3:c.976+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000392434
  ensembl transcript: ENST00000451404
  gene symbol: SLC2A8
  hgvsc: ENST00000451404.1:c.487+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000389070
  ensembl transcript: ENST00000423934
  gene symbol: SLC2A8
  hgvsc: ENST00000423934.1:c.571+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000391213
  ensembl transcript: ENST00000430147
  gene symbol: SLC2A8
  hgvsc: ENST00000430147.1:c.493+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000489239
  gene symbol: SLC2A8
  hgvsc: ENST00000489239.1:n.635+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl transcript: ENST00000477027
  gene symbol: SLC2A8
  hgvsc: ENST00000477027.1:n.45+41G>A
  variant of: http://identifiers.org/hgnc/13812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136856
  ensembl protein: ENSP00000362450
  ensembl transcript: ENST00000373352
  gene symbol: SLC2A8
  hgvsc: ENST00000373352.1:c.187+41G>A
  variant of: http://identifiers.org/hgnc/13812
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15666
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1960
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 381
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4758
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4841
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25252
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.24687656171914e-5
allele num: 16008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62200
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

DP
type: SiteQuality
SIO_000300: 1.315124e6

MQRankSum
type: SiteQuality
SIO_000300: -1.317e0

VQSLOD
type: SiteQuality
SIO_000300: -7.991e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.196e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.42e-1

GenotypeQuality
all individuals: 2434
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4701
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.69548999660902e-4
allele num: 5898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.416e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.177e0

DP
type: SiteQuality
SIO_000300: 1.342004e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.355e0

MQ
type: SiteQuality
SIO_000300: 5.685e1

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3712
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.233636703652911e-5
allele num: 16042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 4.272e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

DP
type: SiteQuality
SIO_000300: 1.344672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4653
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62496
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.233636703652911e-5
allele num: 16042
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.344672e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.373e1

FS
type: SiteQuality
SIO_000300: 4.272e0

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 181
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3712
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.600102406554019e-5
allele num: 62496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.373e1

FS
type: SiteQuality
SIO_000300: 4.272e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.22e-1

DP
type: SiteQuality
SIO_000300: 1.344672e6

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

GenotypeQuality
all individuals: 189
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32031
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3515
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.231306081754735e-5
allele num: 16048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.033e0

FS
type: SiteQuality
SIO_000300: 2.772e0

MQ
type: SiteQuality
SIO_000300: 5.67e1

VQSLOD
type: SiteQuality
SIO_000300: -3.065e0

DP
type: SiteQuality
SIO_000300: 1.358714e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.02e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.033e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 1621
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11116
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63232
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16098
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.201923076923077e-3
allele num: 832
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

QD
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ReadPosRankSum
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DP
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VQSLOD
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FS
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.468e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63302
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

Latino
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allele count: 6
allele frequency: 5.390835579514825e-4
allele num: 11130
num of homozygotes: 0

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

FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.848e1

QD
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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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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64086
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

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

European (Finnish)
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allele count: 2
allele frequency: 3.33889816360601e-4
allele num: 5990
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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SIO_000300: -9.1e-2

VQSLOD
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BaseQRankSum
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SIO_000300: -1.268e0

MQ
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SIO_000300: 5.839e1

InbreedingCoeff
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SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

QD
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SIO_000300: 9.220000000000001e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16308
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543352779578356e-5
allele num: 64794
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.89e-2

FS
type: SiteQuality
SIO_000300: 1.516e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
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SIO_000300: -3.956e0

QD
type: SiteQuality
SIO_000300: 9.94e0

DP
type: SiteQuality
SIO_000300: 1.509972e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.540879534038029e-5
allele num: 64898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.17096018735363e-3
allele num: 854
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.174e0

InbreedingCoeff
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SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.046e1

DP
type: SiteQuality
SIO_000300: 1.516247e6

MQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.734e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.904912836767037e-5
allele num: 10096
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64946
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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MQ
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QD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-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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GenotypeQuality
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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: 16364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6122
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European (Non-Finnish)
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allele count: 9
allele frequency: 1.383976626172536e-4
allele num: 65030
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.073329645337759e-5
allele num: 65076
num of homozygotes: 0

Latino
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African
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Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6128
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.485130111524163e-4
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.732099196646873e-5
allele num: 11452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.607445632141541e-5
allele num: 65112
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.838646202282565e-5
allele num: 10164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.103515625e-5
allele num: 16384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

DP
type: SiteQuality
SIO_000300: 1.528299e6

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.102e1

MQ
type: SiteQuality
SIO_000300: 5.875e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

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

GenotypeQuality
all individuals: 1111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48114
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 8.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65140
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: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.519e0

DP
type: SiteQuality
SIO_000300: 1.530598e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

QD
type: SiteQuality
SIO_000300: 7.15e0

VQSLOD
type: SiteQuality
SIO_000300: -2.621e0

MQ
type: SiteQuality
SIO_000300: 5.824e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

GenotypeQuality
all individuals: 48096
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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: 200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535107918086642e-5
allele num: 65142
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.903e1

DP
type: SiteQuality
SIO_000300: 1.530561e6

VQSLOD
type: SiteQuality
SIO_000300: -8.487e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.209e0

FS
type: SiteQuality
SIO_000300: 1.574e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

QD
type: SiteQuality
SIO_000300: 8.460000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

GenotypeQuality
all individuals: 366
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1259
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variant carriers: 0

GenotypeQuality
all individuals: 203
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variant carriers: 0

GenotypeQuality
all individuals: 6323
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
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variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48268
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533883486210388e-5
allele num: 65194
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.806e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

MQ
type: SiteQuality
SIO_000300: 5.296e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

FS
type: SiteQuality
SIO_000300: 9.76e-1

QD
type: SiteQuality
SIO_000300: 3.93e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e-1

DP
type: SiteQuality
SIO_000300: 1.533485e6

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
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GenotypeQuality
all individuals: 786
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 408
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 6090
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.233616037008481e-4
allele num: 64850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.904912836767037e-5
allele num: 10096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.844e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

DP
type: SiteQuality
SIO_000300: 1.525084e6

FS
type: SiteQuality
SIO_000300: 1.112e0

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.848e1

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeQuality
all individuals: 1192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6065
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
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GenotypeQuality
all individuals: 47193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
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GenotypeQuality
all individuals: 440
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GenotypeQuality
all individuals: 828
bin: 9.75e1
variant carriers: 73

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 46
allele frequency: 2.817246447819696e-3
allele num: 16328
num of homozygotes: 1

African
type: Population
allele count: 25
allele frequency: 2.4786833234186e-3
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.631058968817536e-5
allele num: 64780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.748906386701662e-5
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

FS
type: SiteQuality
SIO_000300: 5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.525455e6

QD
type: SiteQuality
SIO_000300: 1.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

GenotypeQuality
all individuals: 247
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
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GenotypeQuality
all individuals: 763
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
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GenotypeQuality
all individuals: 32
bin: 2.5e0
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GenotypeQuality
all individuals: 47444
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GenotypeQuality
all individuals: 6079
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GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 1612
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.330459100442787e-4
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.71771679066465e-5
allele num: 64786
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

FS
type: SiteQuality
SIO_000300: 3.281e0

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.82e1

DP
type: SiteQuality
SIO_000300: 1.52306e6

VQSLOD
type: SiteQuality
SIO_000300: -1.422e0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
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GenotypeQuality
all individuals: 759
bin: 9.75e1
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GenotypeQuality
all individuals: 138
bin: 4.75e1
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GenotypeQuality
all individuals: 977
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GenotypeQuality
all individuals: 417
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GenotypeQuality
all individuals: 160
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 18
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.628343978524484e-5
allele num: 64818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.003e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

FS
type: SiteQuality
SIO_000300: 2.942e0

DP
type: SiteQuality
SIO_000300: 1.521293e6

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 1.051e1

GenotypeQuality
all individuals: 229
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
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GenotypeQuality
all individuals: 6059
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.768853034023149e-5
allele num: 11404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.512764e6

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

FS
type: SiteQuality
SIO_000300: 4.698e0

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547891771407343e-5
allele num: 64604
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.237e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

FS
type: SiteQuality
SIO_000300: 4.698e0

DP
type: SiteQuality
SIO_000300: 1.512764e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573465084809768e-5
allele num: 63554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.547e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

DP
type: SiteQuality
SIO_000300: 1.458938e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.64e-1

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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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: 751
bin: 9.75e1
variant carriers: 8

South Asian
type: Population
allele count: 2
allele frequency: 1.264542235710673e-4
allele num: 15816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.73260766682442e-4
allele num: 8452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.204819277108434e-3
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573465084809768e-5
allele num: 63554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 2.547e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

DP
type: SiteQuality
SIO_000300: 1.458938e6

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.64e-1

QD
type: SiteQuality
SIO_000300: 1.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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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
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5584
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GenotypeQuality
all individuals: 43200
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.721732561067741e-5
allele num: 63536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5978
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15790
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.83e-1

FS
type: SiteQuality
SIO_000300: 6.427e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 1.454643e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.279e0

QD
type: SiteQuality
SIO_000300: 1.902e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 170
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GenotypeQuality
all individuals: 38478
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.429214350006429e-5
allele num: 15554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.596e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.628e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.06e1

DP
type: SiteQuality
SIO_000300: 1.387615e6

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.533385600418136e-5
allele num: 15306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9428
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.838e0

VQSLOD
type: SiteQuality
SIO_000300: -1.886e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

DP
type: SiteQuality
SIO_000300: 1.288304e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.88e-1

QD
type: SiteQuality
SIO_000300: 8.85e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 355
bin: 4.75e1
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GenotypeQuality
all individuals: 734
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.686279753944904e-5
allele num: 14956
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60774
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

MQ
type: SiteQuality
SIO_000300: 5.838e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

FS
type: SiteQuality
SIO_000300: 2.944e0

BaseQRankSum
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SIO_000300: -2.187e0

VQSLOD
type: SiteQuality
SIO_000300: -1.728e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

DP
type: SiteQuality
SIO_000300: 1.153632e6

GenotypeDepth
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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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 677
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.6461989266783e-5
allele num: 60746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.142e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

DP
type: SiteQuality
SIO_000300: 1.152379e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 730
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.486628778633939e-5
allele num: 57362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14156
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

FS
type: SiteQuality
SIO_000300: 1.6279e1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.863e1

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

DP
type: SiteQuality
SIO_000300: 1.026225e6

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1844
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GenotypeQuality
all individuals: 1146
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.853224610822832e-5
allele num: 53960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3886
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.274534794799898e-4
allele num: 7846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6784
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13328
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.791e0

DP
type: SiteQuality
SIO_000300: 9.77827e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.733e0

QD
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.735e0

GenotypeQuality
all individuals: 2230
bin: 6.25e1
variant carriers: 37

GenotypeQuality
all individuals: 17356
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variant carriers: 201

GenotypeQuality
all individuals: 62
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variant carriers: 10

GenotypeQuality
all individuals: 9592
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variant carriers: 222

GenotypeQuality
all individuals: 838
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variant carriers: 62

GenotypeQuality
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variant carriers: 178

GenotypeQuality
all individuals: 790
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variant carriers: 104

GenotypeQuality
all individuals: 3579
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variant carriers: 262

GenotypeQuality
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variant carriers: 219

GenotypeQuality
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variant carriers: 125

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 17

GenotypeQuality
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GenotypeQuality
all individuals: 1241
bin: 3.75e1
variant carriers: 131

GenotypeQuality
all individuals: 686
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variant carriers: 49

GenotypeQuality
all individuals: 157
bin: 7.75e1
variant carriers: 21

GenotypeQuality
all individuals: 260
bin: 9.75e1
variant carriers: 69

European (Finnish)
type: Population
allele count: 57
allele frequency: 3.131868131868132e-2
allele num: 1820
num of homozygotes: 0

East Asian
type: Population
allele count: 56
allele frequency: 1.396508728179551e-2
allele num: 4010
num of homozygotes: 0

South Asian
type: Population
allele count: 174
allele frequency: 2.413984461709212e-2
allele num: 7208
num of homozygotes: 0

Latino
type: Population
allele count: 70
allele frequency: 1.340482573726542e-2
allele num: 5222
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 2.216748768472906e-2
allele num: 406
num of homozygotes: 0

African
type: Population
allele count: 74
allele frequency: 1.470003972983711e-2
allele num: 5034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 649
allele frequency: 1.855558096980787e-2
allele num: 34976
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.717e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: -7.603e0

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.74e-2

DP
type: SiteQuality
SIO_000300: 9.00435e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.905e0

FS
type: SiteQuality
SIO_000300: 4.3299e1

QD
type: SiteQuality
SIO_000300: 9.9e-1

GenotypeQuality
all individuals: 68
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
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GenotypeQuality
all individuals: 1150
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variant carriers: 0

GenotypeQuality
all individuals: 2995
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GenotypeQuality
all individuals: 261
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variant carriers: 0

GenotypeQuality
all individuals: 304
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GenotypeQuality
all individuals: 6452
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 458
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 39
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 327
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12434
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.14e-1

DP
type: SiteQuality
SIO_000300: 8.70263e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.203e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.913e0

GenotypeQuality
all individuals: 467
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 406
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variant carriers: 0

GenotypeQuality
all individuals: 3792
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GenotypeQuality
all individuals: 24956
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GenotypeQuality
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GenotypeQuality
all individuals: 1881
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GenotypeQuality
all individuals: 68
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GenotypeQuality
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GenotypeQuality
all individuals: 487
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GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 91
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GenotypeQuality
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GenotypeQuality
all individuals: 985
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GenotypeQuality
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GenotypeQuality
all individuals: 1408
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GenotypeQuality
all individuals: 14569
bin: 7.5e0
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 7.827448251869891e-4
allele num: 11498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

VQSLOD
type: SiteQuality
SIO_000300: -1.892e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

DP
type: SiteQuality
SIO_000300: 8.18694e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.845e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.67e-2

QD
type: SiteQuality
SIO_000300: 1.112e1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
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GenotypeQuality
all individuals: 3091
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1425
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GenotypeQuality
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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: 16267
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1498
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2292
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.196836555360281e-4
allele num: 4552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.523e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 7.94152e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.404e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

FS
type: SiteQuality
SIO_000300: 2.304e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3402
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GenotypeQuality
all individuals: 64
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.655468838366701e-5
allele num: 35364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.4330900243309e-4
allele num: 4110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.256e0

FS
type: SiteQuality
SIO_000300: 4.238e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.107e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 7.38732e5

QD
type: SiteQuality
SIO_000300: 2.9e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35364
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.833e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.256e0

ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: -7.42e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.38732e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.107e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

African
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1334
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 2336
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.28515111695138e-5
allele num: 30440
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.06056e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.92e-1

VQSLOD
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SIO_000300: 5.82e-1

BaseQRankSum
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SIO_000300: -7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.99e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

South Asian
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allele frequency: 0.0e0
allele num: 6742
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

African
type: Population
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allele frequency: 4.887585532746823e-4
allele num: 2046
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 3.835532371893219e-5
allele num: 26072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1726
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.78674e5

QD
type: SiteQuality
SIO_000300: 2.628e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.33e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28938
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.282380097460887e-4
allele num: 7798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2072
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.76e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.843e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.48e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

QD
type: SiteQuality
SIO_000300: 3.22e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 6.82216e5

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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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: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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: 2466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1342
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.64e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.019e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.434e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

DP
type: SiteQuality
SIO_000300: 6.79141e5

GenotypeQuality
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bin: 5.25e1
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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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 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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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2124
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.79141e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.64e-2

GenotypeQuality
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variant carriers: 20

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

GenotypeQuality
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variant carriers: 2

Latino
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allele count: 3
allele frequency: 2.11864406779661e-3
allele num: 1416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 4.099368697220628e-4
allele num: 24394
num of homozygotes: 0

African
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allele count: 4
allele frequency: 2.094240837696335e-3
allele num: 1910
num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 7.380073800738007e-4
allele num: 5420
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 2.949852507374631e-3
allele num: 678
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 3.221649484536082e-3
allele num: 1552
num of homozygotes: 0

Other
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allele count: 1
allele frequency: 3.90625e-3
allele num: 256
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.6599e1

MQ
type: SiteQuality
SIO_000300: 5.831e1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 9.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 6.72145e5

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.037667071688943e-4
allele num: 6584
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3686
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49280
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.82262e5

MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.842e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.691e1

GenotypeQuality
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variant carriers: 4

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

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

Latino
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allele frequency: 0.0e0
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African
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FS
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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DP
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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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GenotypeQuality
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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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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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InbreedingCoeff
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DP
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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African
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Other
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.899840413405274e-5
allele num: 52636
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

East Asian
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African
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Latino
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allele num: 9020
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 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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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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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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Other
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African
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European (Finnish)
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East Asian
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Latino
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 757
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.824969400244798e-5
allele num: 52288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4084
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.453e0

FS
type: SiteQuality
SIO_000300: 6.69e0

DP
type: SiteQuality
SIO_000300: 9.30549e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.734e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 5.586e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.123e0

QD
type: SiteQuality
SIO_000300: 1.064e1

GenotypeQuality
all individuals: 1687
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 2.5e0
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.893007231287623e-5
allele num: 52826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.017e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.734e0

MQ
type: SiteQuality
SIO_000300: 5.604e1

DP
type: SiteQuality
SIO_000300: 9.34298e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.553e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4160
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.017e0

MQ
type: SiteQuality
SIO_000300: 5.604e1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.734e0

QD
type: SiteQuality
SIO_000300: 1.553e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.34298e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 20

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1984
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 667
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variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 3.594536304816679e-4
allele num: 52858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13806
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.702e-1

FS
type: SiteQuality
SIO_000300: 1.108e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.519e0

QD
type: SiteQuality
SIO_000300: 1.692e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.679e1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 9.37325e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
all individuals: 5989
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5060
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variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2092
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.293946024799416e-5
allele num: 13710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7418
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.477611940298508e-4
allele num: 6700
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52836
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

MQ
type: SiteQuality
SIO_000300: 5.465e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

DP
type: SiteQuality
SIO_000300: 9.51075e5

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

FS
type: SiteQuality
SIO_000300: 9.887e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2092
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8012
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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: 1683
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variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52836
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.492537313432836e-4
allele num: 6700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9100
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.51075e5

FS
type: SiteQuality
SIO_000300: 9.887e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

MQ
type: SiteQuality
SIO_000300: 5.465e1

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

QD
type: SiteQuality
SIO_000300: 9.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 17107
bin: 2.25e1
variant carriers: 2

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7855
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GenotypeQuality
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GenotypeQuality
all individuals: 798
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variant carriers: 37

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 27
allele frequency: 3.666485605649104e-3
allele num: 7364
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.827458185019328e-5
allele num: 52254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.4360499702558e-5
allele num: 13448
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.485e1

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

DP
type: SiteQuality
SIO_000300: 9.58726e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.35e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeQuality
all individuals: 5034
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6975
bin: 6.25e1
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 222
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
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GenotypeQuality
all individuals: 798
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.827458185019328e-5
allele num: 52254
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.35e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.306e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.485e1

DP
type: SiteQuality
SIO_000300: 9.58726e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 2.5e0
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GenotypeQuality
all individuals: 2081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5858
bin: 2.75e1
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GenotypeQuality
all individuals: 798
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2590
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17107
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1793
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.35795763172189e-4
allele num: 7364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.485e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

DP
type: SiteQuality
SIO_000300: 9.58726e5

GenotypeQuality
all individuals: 1511
bin: 1.75e1
variant carriers: 1496

GenotypeQuality
all individuals: 4619
bin: 3.25e1
variant carriers: 4585

GenotypeQuality
all individuals: 913
bin: 9.25e1
variant carriers: 912

GenotypeQuality
all individuals: 3428
bin: 6.75e1
variant carriers: 3423

GenotypeQuality
all individuals: 8467
bin: 9.75e1
variant carriers: 8465

GenotypeQuality
all individuals: 5767
bin: 5.25e1
variant carriers: 5766

GenotypeQuality
all individuals: 672
bin: 1.25e1
variant carriers: 663

GenotypeQuality
all individuals: 714
bin: 7.5e0
variant carriers: 684

GenotypeQuality
all individuals: 1738
bin: 2.75e1
variant carriers: 1716

GenotypeQuality
all individuals: 1468
bin: 7.25e1
variant carriers: 1466

GenotypeQuality
all individuals: 6292
bin: 4.75e1
variant carriers: 6289

GenotypeQuality
all individuals: 3185
bin: 4.25e1
variant carriers: 3181

GenotypeQuality
all individuals: 1528
bin: 8.25e1
variant carriers: 1525

GenotypeQuality
all individuals: 5785
bin: 3.75e1
variant carriers: 5772

GenotypeQuality
all individuals: 2233
bin: 7.75e1
variant carriers: 2231

GenotypeQuality
all individuals: 649
bin: 8.75e1
variant carriers: 648

European (Finnish)
type: Population
allele count: 4327
allele frequency: 9.780741410488246e-1
allele num: 4424
num of homozygotes: 2117

Latino
type: Population
allele count: 9610
allele frequency: 9.693362921121647e-1
allele num: 9914
num of homozygotes: 4655

European (Non-Finnish)
type: Population
allele count: 54713
allele frequency: 9.598098379061119e-1
allele num: 57004
num of homozygotes: 26241

Other
type: Population
allele count: 695
allele frequency: 9.366576819407008e-1
allele num: 742
num of homozygotes: 324

South Asian
type: Population
allele count: 14149
allele frequency: 9.545945216569963e-1
allele num: 14822
num of homozygotes: 6760

African
type: Population
allele count: 7579
allele frequency: 9.15780570323828e-1
allele num: 8276
num of homozygotes: 3471

East Asian
type: Population
allele count: 5626
allele frequency: 7.930645616013533e-1
allele num: 7094
num of homozygotes: 2202

QD
type: SiteQuality
SIO_000300: 3.404e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.623e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.086379e6

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

GenotypeQuality
all individuals: 4210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1439
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18538
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 530
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 696
bin: 7.75e1
variant carriers: 1

Other
type: Population
allele count: 1
allele frequency: 1.41643059490085e-3
allele num: 706
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.45602795573675e-4
allele num: 6868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.363770250368188e-5
allele num: 54320
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14164
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.175275190516511e-4
allele num: 9448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7996
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.348e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

QD
type: SiteQuality
SIO_000300: 1.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

MQ
type: SiteQuality
SIO_000300: 5.52e1

DP
type: SiteQuality
SIO_000300: 1.040165e6

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

GenotypeQuality
all individuals: 1585
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8409
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 621
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5405
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1576
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 696
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 475
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 530
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 429
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18538
bin: 9.75e1
variant carriers: 74

European (Finnish)
type: Population
allele count: 3
allele frequency: 6.744604316546763e-4
allele num: 4448
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.9120559114735e-4
allele num: 6868
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.587637595258256e-3
allele num: 9448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 8.468335787923417e-4
allele num: 54320
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.824060999717594e-4
allele num: 14164
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 1.000500250125062e-3
allele num: 7996
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.41643059490085e-3
allele num: 706
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.958e1

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

MQ
type: SiteQuality
SIO_000300: 5.52e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.348e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.040165e6

GenotypeQuality
all individuals: 1494
bin: 7.5e0
variant carriers: 235

GenotypeQuality
all individuals: 1585
bin: 4.25e1
variant carriers: 335

GenotypeQuality
all individuals: 1684
bin: 4.75e1
variant carriers: 604

GenotypeQuality
all individuals: 4210
bin: 3.75e1
variant carriers: 598

GenotypeQuality
all individuals: 926
bin: 1.25e1
variant carriers: 201

GenotypeQuality
all individuals: 5311
bin: 3.25e1
variant carriers: 512

GenotypeQuality
all individuals: 5405
bin: 6.25e1
variant carriers: 440

GenotypeQuality
all individuals: 1576
bin: 2.5e0
variant carriers: 54

GenotypeQuality
all individuals: 3377
bin: 2.75e1
variant carriers: 244

GenotypeQuality
all individuals: 530
bin: 7.25e1
variant carriers: 224

GenotypeQuality
all individuals: 18538
bin: 9.75e1
variant carriers: 17505

GenotypeQuality
all individuals: 1439
bin: 6.75e1
variant carriers: 355

GenotypeQuality
all individuals: 475
bin: 9.25e1
variant carriers: 335

GenotypeQuality
all individuals: 621
bin: 8.25e1
variant carriers: 386

GenotypeQuality
all individuals: 696
bin: 7.75e1
variant carriers: 351

GenotypeQuality
all individuals: 429
bin: 8.75e1
variant carriers: 305

European (Finnish)
type: Population
allele count: 1817
allele frequency: 4.084982014388489e-1
allele num: 4448
num of homozygotes: 362

European (Non-Finnish)
type: Population
allele count: 12423
allele frequency: 2.2870029455081e-1
allele num: 54320
num of homozygotes: 1433

African
type: Population
allele count: 1467
allele frequency: 1.834667333666833e-1
allele num: 7996
num of homozygotes: 142

East Asian
type: Population
allele count: 1833
allele frequency: 2.668899242865463e-1
allele num: 6868
num of homozygotes: 233

Latino
type: Population
allele count: 5077
allele frequency: 5.373624047417442e-1
allele num: 9448
num of homozygotes: 1391

South Asian
type: Population
allele count: 2385
allele frequency: 1.683846371081615e-1
allele num: 14164
num of homozygotes: 234

Other
type: Population
allele count: 172
allele frequency: 2.436260623229462e-1
allele num: 706
num of homozygotes: 22

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

DP
type: SiteQuality
SIO_000300: 1.040165e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.348e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.52e1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

QD
type: SiteQuality
SIO_000300: 1.958e1

GenotypeQuality
all individuals: 1945
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6653
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15005
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8998
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14366
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.442169022209403e-4
allele num: 6934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55284
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.142e1

MQRankSum
type: SiteQuality
SIO_000300: -2.646e0

MQ
type: SiteQuality
SIO_000300: 4.331e1

DP
type: SiteQuality
SIO_000300: 9.95947e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

FS
type: SiteQuality
SIO_000300: 3.59e0

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeQuality
all individuals: 2894
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9361
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7486
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5870
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 7.75e1
variant carriers: 0