16-16180870-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180870
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180869
    reference: chr 16
allele count: 1
allele frequency: 8.545985950399098e-6
allele num: 117014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+24delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+24delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3390delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+24delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+24delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3390delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+24delT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+24delT
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6473
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: CT
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

16-16180870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180870
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180870
    reference: chr 16
allele count: 1
allele frequency: 8.545985950399098e-6
allele num: 117014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3392C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3392C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+22C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22328
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5816
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

16-16180883-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180883
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180883
    reference: chr 16
allele count: 2
allele frequency: 1.735779625418757e-5
allele num: 115222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3379C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+35C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3379C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+35C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+35C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+35C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+35C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+35C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8326
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-16180884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180884
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180884
    reference: chr 16
allele count: 1
allele frequency: 8.702311333890281e-6
allele num: 114912
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+36G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3378G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+36G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+36G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+36G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3378G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+36G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+36G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14322
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6486
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

16-16180888-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180888
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180888
    reference: chr 16
allele count: 3
allele frequency: 2.631209654785293e-5
allele num: 114016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+40C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+40C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+40C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+40C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3374C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+40C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3374C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+40C>G
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16638
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7232
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS

16-16180888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180888
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180888
    reference: chr 16
allele count: 2
allele frequency: 1.754139769856862e-5
allele num: 114016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3374C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+40C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+40C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3374C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+40C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+40C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+40C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+40C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16636
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7232
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6541
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8404
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

16-16180889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180889
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180889
    reference: chr 16
allele count: 1
allele frequency: 8.820053273121769e-6
allele num: 113378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3373G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+41G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+41G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3373G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+41G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+41G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+41G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+41G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17082
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15784
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-16180893-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180893
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180893
    reference: chr 16
allele count: 1
allele frequency: 8.854729310924966e-6
allele num: 112934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+45T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+45T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+45T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+45T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+45T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3369T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3369T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+45T>C
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7468
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-16180896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16180896
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16180896
    reference: chr 16
allele count: 1689
allele frequency: 1.508870982150834e-2
allele num: 111938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2155+48G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2460+48G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-3366G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2283+48G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-3366G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2460+48G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.700+48G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2460+48G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 1.25e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 17185
  bin: 1.75e1
  variant carriers: 482
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 7.5e0
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 2.75e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14608
  bin: 2.25e1
  variant carriers: 382
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 3.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 7.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 4381
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7479
  bin: 3.25e1
  variant carriers: 2
num of homozygotes: 21
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-16184217-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184217
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184215
    reference: chr 16
allele count: 1
allele frequency: 1.176359872012046e-5
allele num: 85008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-40_2156-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-40_701-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-40_2461-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-40_2116-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-40_2461-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-40_2284-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-40_2293-39delCA
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-40_2461-39delCA
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8310
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10820
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: TCA
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

16-16184222-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184222
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184220
    reference: chr 16
allele count: 2708
allele frequency: 3.116942909760589e-2
allele num: 86880
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-39_2461-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-39_701-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-39_2156-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-39_2284-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-39_2293-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-39_2116-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-39_2461-38delAT
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-39_2461-38delAT
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 2.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 3.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 18692
  bin: 1.25e1
  variant carriers: 747
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 1.75e1
  variant carriers: 858
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 2.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 12746
  bin: 7.5e0
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 2.25e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 7.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 2.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 7814
  bin: 6.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 4781
  bin: 9.75e1
  variant carriers: 2730
num of homozygotes: 68
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: CAT
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

16-16184223-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184223
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184223
    reference: chr 16
allele count: 1
allele frequency: 1.218115818452018e-5
allele num: 82094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-39A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-39A>G
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7544
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4539
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

16-16184227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184227
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184227
    reference: chr 16
allele count: 4
allele frequency: 4.536484678023e-5
allele num: 88174
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-35G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-35G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12653
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17885
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12190
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8011
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4507
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6569
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-16184232-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184232
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184232
    reference: chr 16
allele count: 85057
allele frequency: 8.231906780481195e-1
allele num: 103326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-30C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-30C>G
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 7.5e0
  variant carriers: 5043
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.25e1
  variant carriers: 522
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 2.5e0
  variant carriers: 797
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 1.25e1
  variant carriers: 10646
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 363
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 2.75e1
  variant carriers: 6230
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 1571
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 14580
  bin: 1.75e1
  variant carriers: 14344
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 708
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 1030
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 2.25e1
  variant carriers: 11440
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 3.25e1
  variant carriers: 3116
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 257
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 2.25e1
  variant carriers: 1603
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 9.25e1
  variant carriers: 1299
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 3.25e1
  variant carriers: 2320
genotype quality: GenotypeQuality
  all individuals: 1768
  bin: 8.25e1
  variant carriers: 1762
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 4.75e1
  variant carriers: 3823
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 7.5e0
  variant carriers: 503
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 2.75e1
  variant carriers: 1059
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 7.75e1
  variant carriers: 2086
num of homozygotes: 34815
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/16-16184234-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184234
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184234
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 104844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-28C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-28C>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2749
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3539
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-16184235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184235
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184235
    reference: chr 16
allele count: 4383
allele frequency: 4.178265014299333e-2
allele num: 104900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-27G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-27G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 3.25e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.5e0
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 3.75e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 14984
  bin: 2.25e1
  variant carriers: 1023
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 7.5e0
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 1.75e1
  variant carriers: 1058
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 10606
  bin: 1.25e1
  variant carriers: 662
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 2.75e1
  variant carriers: 645
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 8.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 3.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 18069
  bin: 6.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 3245
  bin: 6.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 1.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 4270
  bin: 3.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 1.25e1
  variant carriers: 18
num of homozygotes: 131
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-16184240-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184240
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184240
    reference: chr 16
allele count: 1
allele frequency: 9.48622599984822e-6
allele num: 105416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-22C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-22C>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9480
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4359
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

16-16184240-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184240
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184240
    reference: chr 16
allele count: 6
allele frequency: 5.691735599908932e-5
allele num: 105416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-22C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-22C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18141
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10339
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-16184242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184242
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184242
    reference: chr 16
allele count: 1
allele frequency: 9.440731090215627e-6
allele num: 105924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-20G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-20G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4256
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6276
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

16-16184247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184247
    reference: chr 16
allele count: 1
allele frequency: 9.400263207369806e-6
allele num: 106380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.701-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2293-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2461-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2156-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2461-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2461-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2116-15C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2284-15C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3906
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3876
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

16-16184278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184278
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184278
    reference: chr 16
allele count: 2
allele frequency: 1.796719190757676e-5
allele num: 111314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.717C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2477C>T
  hgvsp: ENSP00000382342.3:p.Thr826Met
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2132C>T
  hgvsp: ENSP00000263016.8:p.Thr711Met
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2300C>T
  hgvsp: ENSP00000263017.5:p.Thr767Met
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2477C>T
  hgvsp: ENSP00000263014.5:p.Thr826Met
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2477C>T
  hgvsp: ENSP00000382340.2:p.Thr826Met
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2172C>T
  hgvsp: ENSP00000461615.1:p.Thr725Met
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2309C>T
  hgvsp: ENSP00000263019.6:p.Thr770Met
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr826Met
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: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-16184279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184279
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184279
    reference: chr 16
allele count: 3
allele frequency: 2.688364757330274e-5
allele num: 111592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2173G>A
  hgvsp: ENST00000572882.1:c.2173G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.718G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2478G>A
  hgvsp: ENST00000345148.5:c.2478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2133G>A
  hgvsp: ENST00000349029.5:c.2133G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2478G>A
  hgvsp: ENST00000399408.2:c.2478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2310G>A
  hgvsp: ENST00000346370.5:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2478G>A
  hgvsp: ENST00000399410.3:c.2478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2301G>A
  hgvsp: ENST00000351154.5:c.2301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41094
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr826Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-16184293-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184293
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184293
    reference: chr 16
allele count: 5
allele frequency: 4.366507143605687e-5
allele num: 114508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2492A>G
  hgvsp: ENSP00000382340.2:p.Tyr831Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2492A>G
  hgvsp: ENSP00000382342.3:p.Tyr831Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.732A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2147A>G
  hgvsp: ENSP00000263016.8:p.Tyr716Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2324A>G
  hgvsp: ENSP00000263019.6:p.Tyr775Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2315A>G
  hgvsp: ENSP00000263017.5:p.Tyr772Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2492A>G
  hgvsp: ENSP00000263014.5:p.Tyr831Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2187A>G
  hgvsp: ENSP00000461615.1:p.Tyr730Cys
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31644
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43533
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3692
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr831Cys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

16-16184297-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184297
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184297
    reference: chr 16
allele count: 1
allele frequency: 8.679048776254123e-6
allele num: 115220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2496G>C
  hgvsp: ENSP00000382340.2:p.Leu832Phe
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2191G>C
  hgvsp: ENSP00000461615.1:p.Leu731Phe
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2151G>C
  hgvsp: ENSP00000263016.8:p.Leu717Phe
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.736G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2319G>C
  hgvsp: ENSP00000263017.5:p.Leu773Phe
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2328G>C
  hgvsp: ENSP00000263019.6:p.Leu776Phe
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2496G>C
  hgvsp: ENSP00000263014.5:p.Leu832Phe
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2496G>C
  hgvsp: ENSP00000382342.3:p.Leu832Phe
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu832Phe
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-16184298-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184298
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184298
    reference: chr 16
allele count: 1
allele frequency: 8.659808098652533e-6
allele num: 115476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2497C>A
  hgvsp: ENSP00000263014.5:p.Pro833Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2497C>A
  hgvsp: ENSP00000382342.3:p.Pro833Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2329C>A
  hgvsp: ENSP00000263019.6:p.Pro777Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.737C>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2497C>A
  hgvsp: ENSP00000382340.2:p.Pro833Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2320C>A
  hgvsp: ENSP00000263017.5:p.Pro774Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2152C>A
  hgvsp: ENSP00000263016.8:p.Pro718Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2192C>A
  hgvsp: ENSP00000461615.1:p.Pro732Thr
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro833Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

16-16184299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184299
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184299
    reference: chr 16
allele count: 1
allele frequency: 8.645134518293105e-6
allele num: 115672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2321C>T
  hgvsp: ENSP00000263017.5:p.Pro774Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2193C>T
  hgvsp: ENSP00000461615.1:p.Pro732Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2498C>T
  hgvsp: ENSP00000382342.3:p.Pro833Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2498C>T
  hgvsp: ENSP00000382340.2:p.Pro833Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.738C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2498C>T
  hgvsp: ENSP00000263014.5:p.Pro833Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2153C>T
  hgvsp: ENSP00000263016.8:p.Pro718Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2330C>T
  hgvsp: ENSP00000263019.6:p.Pro777Leu
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4828
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro833Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-16184300-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184300
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184300
    reference: chr 16
allele count: 3
allele frequency: 2.587500646875162e-5
allele num: 115942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2194G>A
  hgvsp: ENST00000572882.1:c.2194G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2322G>A
  hgvsp: ENST00000351154.5:c.2322G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2499G>A
  hgvsp: ENST00000399408.2:c.2499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2499G>A
  hgvsp: ENST00000399410.3:c.2499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2154G>A
  hgvsp: ENST00000349029.5:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.739G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2499G>A
  hgvsp: ENST00000345148.5:c.2499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2331G>A
  hgvsp: ENST00000346370.5:c.2331G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17547
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro833Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

16-16184302-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184302
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184302
    reference: chr 16
allele count: 2
allele frequency: 1.714501251585914e-5
allele num: 116652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2333A>T
  hgvsp: ENSP00000263019.6:p.Gln778Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2501A>T
  hgvsp: ENSP00000382342.3:p.Gln834Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2501A>T
  hgvsp: ENSP00000382340.2:p.Gln834Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2196A>T
  hgvsp: ENSP00000461615.1:p.Gln733Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2156A>T
  hgvsp: ENSP00000263016.8:p.Gln719Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2501A>T
  hgvsp: ENSP00000263014.5:p.Gln834Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2324A>T
  hgvsp: ENSP00000263017.5:p.Gln775Leu
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.741A>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln834Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

16-16184303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184303
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184303
    reference: chr 16
allele count: 1
allele frequency: 8.561350638676758e-6
allele num: 116804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2334G>A
  hgvsp: ENST00000346370.5:c.2334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2502G>A
  hgvsp: ENST00000399408.2:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2325G>A
  hgvsp: ENST00000351154.5:c.2325G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2502G>A
  hgvsp: ENST00000399410.3:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2502G>A
  hgvsp: ENST00000345148.5:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2197G>A
  hgvsp: ENST00000572882.1:c.2197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2157G>A
  hgvsp: ENST00000349029.5:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.742G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17939
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln834Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

16-16184305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184305
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184305
    reference: chr 16
allele count: 1
allele frequency: 8.541460248044005e-6
allele num: 117076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2504T>C
  hgvsp: ENSP00000263014.5:p.Val835Ala
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2336T>C
  hgvsp: ENSP00000263019.6:p.Val779Ala
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2159T>C
  hgvsp: ENSP00000263016.8:p.Val720Ala
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2199T>C
  hgvsp: ENSP00000461615.1:p.Val734Ala
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2327T>C
  hgvsp: ENSP00000263017.5:p.Val776Ala
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.744T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2504T>C
  hgvsp: ENSP00000382342.3:p.Val835Ala
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2504T>C
  hgvsp: ENSP00000382340.2:p.Val835Ala
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
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: 32108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val835Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

16-16184309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184309
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184309
    reference: chr 16
allele count: 3
allele frequency: 2.55449591280654e-5
allele num: 117440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.748C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2340C>T
  hgvsp: ENST00000346370.5:c.2340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2508C>T
  hgvsp: ENST00000345148.5:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2508C>T
  hgvsp: ENST00000399410.3:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2331C>T
  hgvsp: ENST00000351154.5:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2508C>T
  hgvsp: ENST00000399408.2:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2203C>T
  hgvsp: ENST00000572882.1:c.2203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2163C>T
  hgvsp: ENST00000349029.5:c.2163C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31268
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18787
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp836Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-16184310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184310
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184310
    reference: chr 16
allele count: 1
allele frequency: 8.505571149102662e-6
allele num: 117570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2204G>A
  hgvsp: ENSP00000461615.1:p.Val736Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.749G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2509G>A
  hgvsp: ENSP00000382340.2:p.Val837Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2509G>A
  hgvsp: ENSP00000382342.3:p.Val837Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2341G>A
  hgvsp: ENSP00000263019.6:p.Val781Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2164G>A
  hgvsp: ENSP00000263016.8:p.Val722Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2509G>A
  hgvsp: ENSP00000263014.5:p.Val837Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2332G>A
  hgvsp: ENSP00000263017.5:p.Val778Ile
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1540
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val837Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-16184313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184313
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184313
    reference: chr 16
allele count: 18
allele frequency: 1.525113536229919e-4
allele num: 118024
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2512A>G
  hgvsp: ENSP00000382340.2:p.Ile838Val
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2207A>G
  hgvsp: ENSP00000461615.1:p.Ile737Val
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.752A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2512A>G
  hgvsp: ENSP00000263014.5:p.Ile838Val
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2512A>G
  hgvsp: ENSP00000382342.3:p.Ile838Val
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2344A>G
  hgvsp: ENSP00000263019.6:p.Ile782Val
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2335A>G
  hgvsp: ENSP00000263017.5:p.Ile779Val
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2167A>G
  hgvsp: ENSP00000263016.8:p.Ile723Val
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19148
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31723
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile838Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-16184314-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184314
    reference: chr 16
allele count: 6
allele frequency: 5.080440304826418e-5
allele num: 118100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2208T>C
  hgvsp: ENSP00000461615.1:p.Ile737Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2168T>C
  hgvsp: ENSP00000263016.8:p.Ile723Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2336T>C
  hgvsp: ENSP00000263017.5:p.Ile779Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2513T>C
  hgvsp: ENSP00000263014.5:p.Ile838Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2345T>C
  hgvsp: ENSP00000263019.6:p.Ile782Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2513T>C
  hgvsp: ENSP00000382340.2:p.Ile838Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2513T>C
  hgvsp: ENSP00000382342.3:p.Ile838Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.753T>C
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19216
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31794
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46815
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile838Thr
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

16-16184317-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184317
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184317
    reference: chr 16
allele count: 1
allele frequency: 8.453514125822104e-6
allele num: 118294
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2516T>G
  hgvsp: ENSP00000382342.3:p.Ile839Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2171T>G
  hgvsp: ENSP00000263016.8:p.Ile724Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2211T>G
  hgvsp: ENSP00000461615.1:p.Ile738Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2339T>G
  hgvsp: ENSP00000263017.5:p.Ile780Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2516T>G
  hgvsp: ENSP00000382340.2:p.Ile839Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.756T>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2348T>G
  hgvsp: ENSP00000263019.6:p.Ile783Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2516T>G
  hgvsp: ENSP00000263014.5:p.Ile839Ser
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile839Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-16184318-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184318
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184318
    reference: chr 16
allele count: 4
allele frequency: 3.381577167590964e-5
allele num: 118288
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2517C>T
  hgvsp: ENST00000399410.3:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2172C>T
  hgvsp: ENST00000349029.5:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2349C>T
  hgvsp: ENST00000346370.5:c.2349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2212C>T
  hgvsp: ENST00000572882.1:c.2212C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2517C>T
  hgvsp: ENST00000399408.2:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2517C>T
  hgvsp: ENST00000345148.5:c.2517C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2340C>T
  hgvsp: ENST00000351154.5:c.2340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.757C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31785
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile839Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-16184319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184319
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184319
    reference: chr 16
allele count: 1
allele frequency: 8.447515585666255e-6
allele num: 118378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2518G>A
  hgvsp: ENSP00000382340.2:p.Val840Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.758G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2173G>A
  hgvsp: ENSP00000263016.8:p.Val725Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2341G>A
  hgvsp: ENSP00000263017.5:p.Val781Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2213G>A
  hgvsp: ENSP00000461615.1:p.Val739Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2518G>A
  hgvsp: ENSP00000382342.3:p.Val840Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2518G>A
  hgvsp: ENSP00000263014.5:p.Val840Ile
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2350G>A
  hgvsp: ENSP00000263019.6:p.Val784Ile
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46402
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val840Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

16-16184326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184326
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184326
    reference: chr 16
allele count: 1
allele frequency: 8.444947387977773e-6
allele num: 118414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2357G>A
  hgvsp: ENSP00000263019.6:p.Ser786Asn
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2220G>A
  hgvsp: ENSP00000461615.1:p.Ser741Asn
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2525G>A
  hgvsp: ENSP00000382342.3:p.Ser842Asn
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2180G>A
  hgvsp: ENSP00000263016.8:p.Ser727Asn
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2525G>A
  hgvsp: ENSP00000382340.2:p.Ser842Asn
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2348G>A
  hgvsp: ENSP00000263017.5:p.Ser783Asn
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.765G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2525G>A
  hgvsp: ENSP00000263014.5:p.Ser842Asn
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31036
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser842Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

16-16184330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184330
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184330
    reference: chr 16
allele count: 4
allele frequency: 3.377294449416573e-5
allele num: 118438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2224C>T
  hgvsp: ENST00000572882.1:c.2224C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2529C>T
  hgvsp: ENST00000399408.2:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2529C>T
  hgvsp: ENST00000399410.3:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2184C>T
  hgvsp: ENST00000349029.5:c.2184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2352C>T
  hgvsp: ENST00000351154.5:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2529C>T
  hgvsp: ENST00000345148.5:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2361C>T
  hgvsp: ENST00000346370.5:c.2361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.769C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31057
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly843Gly
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

16-16184331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184331
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184331
    reference: chr 16
allele count: 22
allele frequency: 1.856352099365465e-4
allele num: 118512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2353G>A
  hgvsp: ENSP00000263017.5:p.Gly785Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2185G>A
  hgvsp: ENSP00000263016.8:p.Gly729Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2362G>A
  hgvsp: ENSP00000263019.6:p.Gly788Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2225G>A
  hgvsp: ENSP00000461615.1:p.Gly743Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2530G>A
  hgvsp: ENSP00000263014.5:p.Gly844Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2530G>A
  hgvsp: ENSP00000382340.2:p.Gly844Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.770G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2530G>A
  hgvsp: ENSP00000382342.3:p.Gly844Ser
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31171
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18905
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4588
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly844Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

16-16184350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184350
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184350
    reference: chr 16
allele count: 1
allele frequency: 8.423180592991915e-6
allele num: 118720
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2549G>A
  hgvsp: ENSP00000382342.3:p.Gly850Asp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.789G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2204G>A
  hgvsp: ENSP00000263016.8:p.Gly735Asp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2549G>A
  hgvsp: ENSP00000263014.5:p.Gly850Asp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2549G>A
  hgvsp: ENSP00000382340.2:p.Gly850Asp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2381G>A
  hgvsp: ENSP00000263019.6:p.Gly794Asp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2372G>A
  hgvsp: ENSP00000263017.5:p.Gly791Asp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2244G>A
  hgvsp: ENSP00000461615.1:p.Gly749Asp
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19578
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
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: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly850Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

16-16184361-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184361
    reference: chr 16
allele count: 3
allele frequency: 2.525210013299439e-5
allele num: 118802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2215G>C
  hgvsp: ENSP00000263016.8:p.Glu739Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.800G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2560G>C
  hgvsp: ENSP00000382340.2:p.Glu854Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2560G>C
  hgvsp: ENSP00000382342.3:p.Glu854Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2383G>C
  hgvsp: ENSP00000263017.5:p.Glu795Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2255G>C
  hgvsp: ENSP00000461615.1:p.Glu753Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2392G>C
  hgvsp: ENSP00000263019.6:p.Glu798Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2560G>C
  hgvsp: ENSP00000263014.5:p.Glu854Gln
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1781
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu854Gln
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-16184364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184364
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184364
    reference: chr 16
allele count: 1
allele frequency: 8.427297702718647e-6
allele num: 118662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2563C>T
  hgvsp: ENST00000399408.2:c.2563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2258C>T
  hgvsp: ENST00000572882.1:c.2258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.803C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2563C>T
  hgvsp: ENST00000399410.3:c.2563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2386C>T
  hgvsp: ENST00000351154.5:c.2386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2563C>T
  hgvsp: ENST00000345148.5:c.2563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2218C>T
  hgvsp: ENST00000349029.5:c.2218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2395C>T
  hgvsp: ENST00000346370.5:c.2395C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu855Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-16184366-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184366
    reference: chr 16
allele count: 195
allele frequency: 1.644015782551512e-3
allele num: 118612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2260G>T
  hgvsp: ENST00000572882.1:c.2260G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2565G>T
  hgvsp: ENST00000345148.5:c.2565G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2565G>T
  hgvsp: ENST00000399410.3:c.2565G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2397G>T
  hgvsp: ENST00000346370.5:c.2397G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2565G>T
  hgvsp: ENST00000399408.2:c.2565G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2220G>T
  hgvsp: ENST00000349029.5:c.2220G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.805G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2388G>T
  hgvsp: ENST00000351154.5:c.2388G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20759
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29771
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44443
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu855Leu
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-16184374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184374
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184374
    reference: chr 16
allele count: 2
allele frequency: 1.688162603822e-5
allele num: 118472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2228G>A
  hgvsp: ENSP00000263016.8:p.Arg743Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2573G>A
  hgvsp: ENSP00000382342.3:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2268G>A
  hgvsp: ENSP00000461615.1:p.Arg757Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2573G>A
  hgvsp: ENSP00000263014.5:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2396G>A
  hgvsp: ENSP00000263017.5:p.Arg799Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2405G>A
  hgvsp: ENSP00000263019.6:p.Arg802Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.813G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2573G>A
  hgvsp: ENSP00000382340.2:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20716
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46822
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg858Gln
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-16184374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184374
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184374
    reference: chr 16
allele count: 5
allele frequency: 4.220406509555e-5
allele num: 118472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2573G>C
  hgvsp: ENSP00000382340.2:p.Arg858Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2573G>C
  hgvsp: ENSP00000263014.5:p.Arg858Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2573G>C
  hgvsp: ENSP00000382342.3:p.Arg858Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2228G>C
  hgvsp: ENSP00000263016.8:p.Arg743Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2268G>C
  hgvsp: ENSP00000461615.1:p.Arg757Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.813G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2405G>C
  hgvsp: ENSP00000263019.6:p.Arg802Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2396G>C
  hgvsp: ENSP00000263017.5:p.Arg799Pro
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30480
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg858Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

16-16184378-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184378
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184378
    reference: chr 16
allele count: 2
allele frequency: 1.688077111362447e-5
allele num: 118478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2400C>T
  hgvsp: ENST00000351154.5:c.2400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2577C>T
  hgvsp: ENST00000399410.3:c.2577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2232C>T
  hgvsp: ENST00000349029.5:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2577C>T
  hgvsp: ENST00000345148.5:c.2577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2577C>T
  hgvsp: ENST00000399408.2:c.2577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2272C>T
  hgvsp: ENST00000572882.1:c.2272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.817C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2409C>T
  hgvsp: ENST00000346370.5:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp859Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-16184379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184379
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184379
    reference: chr 16
allele count: 1
allele frequency: 8.442665856170744e-6
allele num: 118446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2578G>A
  hgvsp: ENSP00000263014.5:p.Gly860Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.818G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2273G>A
  hgvsp: ENSP00000461615.1:p.Gly759Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2233G>A
  hgvsp: ENSP00000263016.8:p.Gly745Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2578G>A
  hgvsp: ENSP00000382342.3:p.Gly860Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2410G>A
  hgvsp: ENSP00000263019.6:p.Gly804Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2578G>A
  hgvsp: ENSP00000382340.2:p.Gly860Ser
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2401G>A
  hgvsp: ENSP00000263017.5:p.Gly801Ser
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly860Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

16-16184381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184381
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184381
    reference: chr 16
allele count: 1
allele frequency: 8.44409166905916e-6
allele num: 118426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2580C>T
  hgvsp: ENST00000399408.2:c.2580C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2412C>T
  hgvsp: ENST00000346370.5:c.2412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2275C>T
  hgvsp: ENST00000572882.1:c.2275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2580C>T
  hgvsp: ENST00000399410.3:c.2580C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2403C>T
  hgvsp: ENST00000351154.5:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2580C>T
  hgvsp: ENST00000345148.5:c.2580C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2235C>T
  hgvsp: ENST00000349029.5:c.2235C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.820C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20787
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly860Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-16184382-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184382
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184382
    reference: chr 16
allele count: 1
allele frequency: 8.446802040747373e-6
allele num: 118388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2413G>A
  hgvsp: ENSP00000263019.6:p.Ala805Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2581G>A
  hgvsp: ENSP00000382340.2:p.Ala861Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2276G>A
  hgvsp: ENSP00000461615.1:p.Ala760Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2581G>A
  hgvsp: ENSP00000382342.3:p.Ala861Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2581G>A
  hgvsp: ENSP00000263014.5:p.Ala861Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2236G>A
  hgvsp: ENSP00000263016.8:p.Ala746Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2404G>A
  hgvsp: ENSP00000263017.5:p.Ala802Thr
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.821G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30667
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47548
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala861Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-16184384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184384
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184384
    reference: chr 16
allele count: 21
allele frequency: 1.7729897673162e-4
allele num: 118444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2583C>T
  hgvsp: ENST00000345148.5:c.2583C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2278C>T
  hgvsp: ENST00000572882.1:c.2278C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2238C>T
  hgvsp: ENST00000349029.5:c.2238C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2415C>T
  hgvsp: ENST00000346370.5:c.2415C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2583C>T
  hgvsp: ENST00000399408.2:c.2583C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2406C>T
  hgvsp: ENST00000351154.5:c.2406C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2583C>T
  hgvsp: ENST00000399410.3:c.2583C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.823C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30741
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20952
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala861Ala
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: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-16184387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184387
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184387
    reference: chr 16
allele count: 3
allele frequency: 2.535968486364943e-5
allele num: 118298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2281C>T
  hgvsp: ENST00000572882.1:c.2281C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2409C>T
  hgvsp: ENST00000351154.5:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.826C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2418C>T
  hgvsp: ENST00000346370.5:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2586C>T
  hgvsp: ENST00000399410.3:c.2586C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2586C>T
  hgvsp: ENST00000345148.5:c.2586C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2241C>T
  hgvsp: ENST00000349029.5:c.2241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2586C>T
  hgvsp: ENST00000399408.2:c.2586C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe862Phe
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-16184389-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184389
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184389
    reference: chr 16
allele count: 1
allele frequency: 8.458805616646929e-6
allele num: 118220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.828C>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2420C>G
  hgvsp: ENSP00000263019.6:p.Ala807Gly
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2588C>G
  hgvsp: ENSP00000382340.2:p.Ala863Gly
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2283C>G
  hgvsp: ENSP00000461615.1:p.Ala762Gly
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2411C>G
  hgvsp: ENSP00000263017.5:p.Ala804Gly
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2243C>G
  hgvsp: ENSP00000263016.8:p.Ala748Gly
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2588C>G
  hgvsp: ENSP00000382342.3:p.Ala863Gly
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2588C>G
  hgvsp: ENSP00000263014.5:p.Ala863Gly
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30848
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48230
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala863Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

16-16184398-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184398
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184398
    reference: chr 16
allele count: 1
allele frequency: 8.508755509419192e-6
allele num: 117526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2252T>C
  hgvsp: ENSP00000263016.8:p.Leu751Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2597T>C
  hgvsp: ENSP00000382342.3:p.Leu866Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.837T>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2420T>C
  hgvsp: ENSP00000263017.5:p.Leu807Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2597T>C
  hgvsp: ENSP00000263014.5:p.Leu866Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2292T>C
  hgvsp: ENSP00000461615.1:p.Leu765Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2597T>C
  hgvsp: ENSP00000382340.2:p.Leu866Pro
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2429T>C
  hgvsp: ENSP00000263019.6:p.Leu810Pro
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu866Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-16184400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184400
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184400
    reference: chr 16
allele count: 6
allele frequency: 5.108121913843011e-5
allele num: 117460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2599C>T
  hgvsp: ENSP00000382340.2:p.Arg867Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2254C>T
  hgvsp: ENSP00000263016.8:p.Arg752Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2599C>T
  hgvsp: ENSP00000382342.3:p.Arg867Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2599C>T
  hgvsp: ENSP00000263014.5:p.Arg867Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2294C>T
  hgvsp: ENSP00000461615.1:p.Arg766Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.839C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2422C>T
  hgvsp: ENSP00000263017.5:p.Arg808Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2431C>T
  hgvsp: ENSP00000263019.6:p.Arg811Cys
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30261
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47648
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg867Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

16-16184401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184401
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184401
    reference: chr 16
allele count: 1
allele frequency: 8.511507558218711e-6
allele num: 117488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2600G>A
  hgvsp: ENSP00000382340.2:p.Arg867His
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2600G>A
  hgvsp: ENSP00000263014.5:p.Arg867His
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.840G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2423G>A
  hgvsp: ENSP00000263017.5:p.Arg808His
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2432G>A
  hgvsp: ENSP00000263019.6:p.Arg811His
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2600G>A
  hgvsp: ENSP00000382342.3:p.Arg867His
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2295G>A
  hgvsp: ENSP00000461615.1:p.Arg766His
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2255G>A
  hgvsp: ENSP00000263016.8:p.Arg752His
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg867His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-16184407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184407
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184407
    reference: chr 16
allele count: 1
allele frequency: 8.547885253188362e-6
allele num: 116988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.846A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2261A>G
  hgvsp: ENSP00000263016.8:p.Tyr754Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2606A>G
  hgvsp: ENSP00000382342.3:p.Tyr869Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2301A>G
  hgvsp: ENSP00000461615.1:p.Tyr768Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2606A>G
  hgvsp: ENSP00000382340.2:p.Tyr869Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2429A>G
  hgvsp: ENSP00000263017.5:p.Tyr810Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2606A>G
  hgvsp: ENSP00000263014.5:p.Tyr869Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2438A>G
  hgvsp: ENSP00000263019.6:p.Tyr813Cys
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr869Cys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-16184408-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184408
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184408
    reference: chr 16
allele count: 1
allele frequency: 8.549493015064207e-6
allele num: 116966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2430T>G
  hgvsp: ENSP00000263017.5:p.Tyr810Ter
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2302T>G
  hgvsp: ENSP00000461615.1:p.Tyr768Ter
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2262T>G
  hgvsp: ENSP00000263016.8:p.Tyr754Ter
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.847T>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2439T>G
  hgvsp: ENSP00000263019.6:p.Tyr813Ter
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2607T>G
  hgvsp: ENSP00000382342.3:p.Tyr869Ter
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2607T>G
  hgvsp: ENSP00000382340.2:p.Tyr869Ter
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2607T>G
  hgvsp: ENSP00000263014.5:p.Tyr869Ter
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47769
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr869Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

16-16184414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184414
    reference: chr 16
allele count: 1
allele frequency: 8.599191675982458e-6
allele num: 116290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2613C>T
  hgvsp: ENST00000399408.2:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2445C>T
  hgvsp: ENST00000346370.5:c.2445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.853C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2436C>T
  hgvsp: ENST00000351154.5:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2268C>T
  hgvsp: ENST00000349029.5:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2308C>T
  hgvsp: ENST00000572882.1:c.2308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2613C>T
  hgvsp: ENST00000399410.3:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2613C>T
  hgvsp: ENST00000345148.5:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21173
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4336
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser871Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

16-16184424-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184424
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184424
    reference: chr 16
allele count: 1
allele frequency: 8.707615680674318e-6
allele num: 114842
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2623G>C
  hgvsp: ENSP00000382342.3:p.Glu875Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.863G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2446G>C
  hgvsp: ENSP00000263017.5:p.Glu816Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2623G>C
  hgvsp: ENSP00000382340.2:p.Glu875Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2623G>C
  hgvsp: ENSP00000263014.5:p.Glu875Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2455G>C
  hgvsp: ENSP00000263019.6:p.Glu819Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2278G>C
  hgvsp: ENSP00000263016.8:p.Glu760Gln
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2318G>C
  hgvsp: ENSP00000461615.1:p.Glu774Gln
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu875Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

16-16184444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184444
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184444
    reference: chr 16
allele count: 3
allele frequency: 2.751132549566238e-5
allele num: 109046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.883C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2475C>T
  hgvsp: ENST00000346370.5:c.2475C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2466C>T
  hgvsp: ENST00000351154.5:c.2466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2643C>T
  hgvsp: ENST00000399410.3:c.2643C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2643C>T
  hgvsp: ENST00000345148.5:c.2643C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2338C>T
  hgvsp: ENST00000572882.1:c.2338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2298C>T
  hgvsp: ENST00000349029.5:c.2298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2643C>T
  hgvsp: ENST00000399408.2:c.2643C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39005
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2643C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-16184445-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184445
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184445
    reference: chr 16
allele count: 1
allele frequency: 9.236680706421341e-6
allele num: 108264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467G>T
  hgvsp: ENSP00000263017.5:p.Gly823Trp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299G>T
  hgvsp: ENSP00000263016.8:p.Gly767Trp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644G>T
  hgvsp: ENSP00000382340.2:p.Gly882Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339G>T
  hgvsp: ENSP00000461615.1:p.Gly781Cys
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644G>T
  hgvsp: ENSP00000382342.3:p.Gly882Trp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476G>T
  hgvsp: ENSP00000263019.6:p.Gly826Trp
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644G>T
  hgvsp: ENSP00000263014.5:p.Gly882Trp
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly882Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-16184455-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184455
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184455
    reference: chr 16
allele count: 1
allele frequency: 9.61686413294353e-6
allele num: 103984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+10G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+10G>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18739
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14981
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-16184455-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184455
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184454
    reference: chr 16
allele count: 1
allele frequency: 9.61686413294353e-6
allele num: 103984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+14delC
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+14delC
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15384
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2650
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: GC
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

16-16184458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184458
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184458
    reference: chr 16
allele count: 2
allele frequency: 1.95545474100002e-5
allele num: 102278
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+13C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+13C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2878
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-16184460-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184460
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184460
    reference: chr 16
allele count: 2
allele frequency: 1.963402183303228e-5
allele num: 101864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+15A>G
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+15A>G
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2975
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-16184462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184462
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184462
    reference: chr 16
allele count: 1
allele frequency: 9.882008814751862e-6
allele num: 101194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+17G>A
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+17G>A
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12633
  bin: 2.75e1
  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: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18282
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-16184462-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184462
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184462
    reference: chr 16
allele count: 2
allele frequency: 1.976401762950372e-5
allele num: 101194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+17G>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+17G>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12633
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18282
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

16-16184463-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184463
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184463
    reference: chr 16
allele count: 1
allele frequency: 9.929894941711517e-6
allele num: 100706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+18G>C
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+18G>C
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15181
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18818
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

16-16184470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184470
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184470
    reference: chr 16
allele count: 1
allele frequency: 1.022160438302396e-5
allele num: 97832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+25C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+25C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  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: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5039
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22271
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

16-16184471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16184471
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 16184471
    reference: chr 16
allele count: 1
allele frequency: 1.02633577601248e-5
allele num: 97434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263016
  ensembl transcript: ENST00000349029
  gene symbol: ABCC1
  hgvsc: ENST00000349029.5:c.2299+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl transcript: ENST00000575422
  gene symbol: ABCC1
  hgvsc: ENST00000575422.1:n.884+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263019
  ensembl transcript: ENST00000346370
  gene symbol: ABCC1
  hgvsc: ENST00000346370.5:c.2476+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000461615
  ensembl transcript: ENST00000572882
  gene symbol: ABCC1
  hgvsc: ENST00000572882.1:c.2339+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263017
  ensembl transcript: ENST00000351154
  gene symbol: ABCC1
  hgvsc: ENST00000351154.5:c.2467+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382340
  ensembl transcript: ENST00000399408
  gene symbol: ABCC1
  hgvsc: ENST00000399408.2:c.2644+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000263014
  ensembl transcript: ENST00000345148
  gene symbol: ABCC1
  hgvsc: ENST00000345148.5:c.2644+26C>T
  variant of: http://identifiers.org/hgnc/51
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103222
  ensembl protein: ENSP00000382342
  ensembl transcript: ENST00000399410
  gene symbol: ABCC1
  hgvsc: ENST00000399410.3:c.2644+26C>T
  variant of: http://identifiers.org/hgnc/51
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9767
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32641
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5816
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543066999969139e-5
allele num: 64806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.444431e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

GenotypeQuality
all individuals: 519
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6473
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32641
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543066999969139e-5
allele num: 64806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

DP
type: SiteQuality
SIO_000300: 1.444431e6

GenotypeQuality
all individuals: 21548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4004
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4190
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5037
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.141786249732277e-4
allele num: 9338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.413e0

DP
type: SiteQuality
SIO_000300: 1.287237e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.36e1

GenotypeQuality
all individuals: 2051
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 427
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20558
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.073883161512027e-4
allele num: 9312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15934
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.367e1

FS
type: SiteQuality
SIO_000300: 4.568e0

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.274648e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.587e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

GenotypeQuality
all individuals: 2771
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 496
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6541
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.74743638435245e-5
allele num: 63192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.63e0

QD
type: SiteQuality
SIO_000300: 1.301e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

DP
type: SiteQuality
SIO_000300: 1.232987e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1087
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2787
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 367
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16638
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.58247879478415e-5
allele num: 63192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.077354018530489e-4
allele num: 9282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.63e0

DP
type: SiteQuality
SIO_000300: 1.232987e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

QD
type: SiteQuality
SIO_000300: 1.301e1

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

GenotypeQuality
all individuals: 979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 582
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7304
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4380
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6746
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590887396990041e-5
allele num: 62858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.366e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

DP
type: SiteQuality
SIO_000300: 1.222423e6

GenotypeQuality
all individuals: 628
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4837
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8062
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4510
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596882884609243e-5
allele num: 62622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15690
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.448e0

VQSLOD
type: SiteQuality
SIO_000300: -4.927e-1

MQ
type: SiteQuality
SIO_000300: 5.685e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 1.198096e6

FS
type: SiteQuality
SIO_000300: 2.258e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 670
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 728
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2542
bin: 9.75e1
variant carriers: 1616

GenotypeQuality
all individuals: 7359
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 7447
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 994
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 9070
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 714
bin: 8.25e1
variant carriers: 18

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 19

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 17

GenotypeQuality
all individuals: 5610
bin: 4.75e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 105
allele frequency: 1.752921535893155e-2
allele num: 5990
num of homozygotes: 1

Latino
type: Population
allele count: 92
allele frequency: 8.832565284178187e-3
allele num: 10416
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.970908624887864e-4
allele num: 15606
num of homozygotes: 0

African
type: Population
allele count: 354
allele frequency: 3.87817703768624e-2
allele num: 9128
num of homozygotes: 11

Other
type: Population
allele count: 14
allele frequency: 1.699029126213592e-2
allele num: 824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1110
allele frequency: 1.789860681114551e-2
allele num: 62016
num of homozygotes: 9

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.505e1

VQSLOD
type: SiteQuality
SIO_000300: 6.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.188929e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7240
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2527
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4808
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4672
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.217433649866082e-4
allele num: 8214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 8.92968e5

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 2.373e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 612
bin: 2.5e0
variant carriers: 17

GenotypeQuality
all individuals: 1541
bin: 1.75e1
variant carriers: 14

GenotypeQuality
all individuals: 841
bin: 7.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1492
bin: 1.25e1
variant carriers: 11

GenotypeQuality
all individuals: 10634
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 6757
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 440
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 3067
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 7891
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 410
bin: 9.25e1
variant carriers: 14

Other
type: Population
allele count: 15
allele frequency: 2.435064935064935e-2
allele num: 616
num of homozygotes: 0

East Asian
type: Population
allele count: 412
allele frequency: 6.229210765043847e-2
allele num: 6614
num of homozygotes: 11

Latino
type: Population
allele count: 912
allele frequency: 1.042047531992687e-1
allele num: 8752
num of homozygotes: 36

European (Finnish)
type: Population
allele count: 111
allele frequency: 2.320234113712374e-2
allele num: 4784
num of homozygotes: 1

African
type: Population
allele count: 393
allele frequency: 5.029434348605068e-2
allele num: 7814
num of homozygotes: 9

South Asian
type: Population
allele count: 48
allele frequency: 7.47896540978498e-3
allele num: 6418
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 817
allele frequency: 1.574727265718361e-2
allele num: 51882
num of homozygotes: 10

BaseQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.898e1

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

DP
type: SiteQuality
SIO_000300: 9.24044e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.32e-2

MQ
type: SiteQuality
SIO_000300: 5.739e1

GenotypeQuality
all individuals: 7880
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6689
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10585
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2729
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.566416040100251e-4
allele num: 6384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.57e1

VQSLOD
type: SiteQuality
SIO_000300: -6.766e-1

DP
type: SiteQuality
SIO_000300: 8.72465e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.431e0

QD
type: SiteQuality
SIO_000300: 1.812e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

GenotypeQuality
all individuals: 1248
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2834
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11289
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 4
allele frequency: 6.105006105006105e-4
allele num: 6552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52420
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 2.966e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 9.49136e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.402e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

QD
type: SiteQuality
SIO_000300: 1.134e1

GenotypeQuality
all individuals: 4094
bin: 6.25e1
variant carriers: 3577

GenotypeQuality
all individuals: 2925
bin: 6.75e1
variant carriers: 2899

GenotypeQuality
all individuals: 1327
bin: 1.75e1
variant carriers: 1267

GenotypeQuality
all individuals: 1086
bin: 2.5e0
variant carriers: 174

GenotypeQuality
all individuals: 3978
bin: 5.25e1
variant carriers: 3953

GenotypeQuality
all individuals: 673
bin: 1.25e1
variant carriers: 583

GenotypeQuality
all individuals: 1965
bin: 4.25e1
variant carriers: 1894

GenotypeQuality
all individuals: 2229
bin: 5.75e1
variant carriers: 2205

GenotypeQuality
all individuals: 20279
bin: 9.75e1
variant carriers: 20258

GenotypeQuality
all individuals: 920
bin: 8.75e1
variant carriers: 917

GenotypeQuality
all individuals: 1526
bin: 7.25e1
variant carriers: 1510

GenotypeQuality
all individuals: 3178
bin: 3.75e1
variant carriers: 3024

Other
type: Population
allele count: 616
allele frequency: 8.279569892473119e-1
allele num: 744
num of homozygotes: 255

South Asian
type: Population
allele count: 6280
allele frequency: 7.032474804031354e-1
allele num: 8930
num of homozygotes: 2161

East Asian
type: Population
allele count: 6598
allele frequency: 8.282701481295506e-1
allele num: 7966
num of homozygotes: 2696

African
type: Population
allele count: 7432
allele frequency: 8.228520814880426e-1
allele num: 9032
num of homozygotes: 3050

European (Non-Finnish)
type: Population
allele count: 50839
allele frequency: 8.427936739498028e-1
allele num: 60322
num of homozygotes: 21316

European (Finnish)
type: Population
allele count: 5007
allele frequency: 8.518203470568221e-1
allele num: 5878
num of homozygotes: 2118

Latino
type: Population
allele count: 8285
allele frequency: 7.925196097187679e-1
allele num: 10454
num of homozygotes: 3219

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 3.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 1.220735e6

GenotypeQuality
all individuals: 1550
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4996
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5265
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4796
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17181
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 9.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.728e0

FS
type: SiteQuality
SIO_000300: 2.237e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

DP
type: SiteQuality
SIO_000300: 1.150065e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.35e-1

GenotypeQuality
all individuals: 902
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 825
bin: 7.25e1
variant carriers: 25

GenotypeQuality
all individuals: 4624
bin: 4.75e1
variant carriers: 30

GenotypeQuality
all individuals: 5363
bin: 2.25e1
variant carriers: 19

GenotypeQuality
all individuals: 1254
bin: 7.5e0
variant carriers: 20

GenotypeQuality
all individuals: 2530
bin: 4.25e1
variant carriers: 13

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 37

GenotypeQuality
all individuals: 4806
bin: 9.75e1
variant carriers: 4065

GenotypeQuality
all individuals: 2670
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3530
bin: 5.25e1
variant carriers: 22

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 27

GenotypeQuality
all individuals: 681
bin: 7.75e1
variant carriers: 35

Other
type: Population
allele count: 23
allele frequency: 3.034300791556728e-2
allele num: 758
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.447381302006853e-4
allele num: 8172
num of homozygotes: 0

African
type: Population
allele count: 93
allele frequency: 1.022202681908112e-2
allele num: 9098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3595
allele frequency: 5.896729324541548e-2
allele num: 60966
num of homozygotes: 116

South Asian
type: Population
allele count: 141
allele frequency: 1.536952256376717e-2
allele num: 9174
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 372
allele frequency: 6.27318718381113e-2
allele num: 5930
num of homozygotes: 13

Latino
type: Population
allele count: 157
allele frequency: 1.453434549157563e-2
allele num: 10802
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.1e0

QD
type: SiteQuality
SIO_000300: 1.542e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.46e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.162324e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

GenotypeQuality
all individuals: 3601
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3752
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.226794611551947e-5
allele num: 10838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.224e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 1.17658e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 7.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

GenotypeQuality
all individuals: 1231
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4655
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3752
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.223091976516634e-4
allele num: 8176
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.246050638389959e-4
allele num: 9242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.1001100110011e-4
allele num: 9090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.630842493232004e-5
allele num: 61318
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
SIO_000300: 1.17658e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

FS
type: SiteQuality
SIO_000300: 7.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

QD
type: SiteQuality
SIO_000300: 1.224e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
all individuals: 3736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2664
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27033
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.218620521569583e-4
allele num: 8206
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.867e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

VQSLOD
type: SiteQuality
SIO_000300: -2.091e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

DP
type: SiteQuality
SIO_000300: 1.191299e6

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

FS
type: SiteQuality
SIO_000300: 2.618e0

QD
type: SiteQuality
SIO_000300: 3.217e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620587949308009e-5
allele num: 61706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

DP
type: SiteQuality
SIO_000300: 1.219685e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.61e-1

FS
type: SiteQuality
SIO_000300: 1.1665e1

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63372
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.371916508538899e-4
allele num: 8432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.794e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e0

VQSLOD
type: SiteQuality
SIO_000300: -1.391e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

DP
type: SiteQuality
SIO_000300: 1.348223e6

GenotypeQuality
all individuals: 4575
bin: 6.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576441655894315e-5
allele num: 63434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.367984844896993e-4
allele num: 8446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.07e1

DP
type: SiteQuality
SIO_000300: 1.353608e6

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 792
bin: 9.75e1
variant carriers: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.637951105937136e-4
allele num: 13744
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

DP
type: SiteQuality
SIO_000300: 1.390696e6

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

QD
type: SiteQuality
SIO_000300: 1.192e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.19e-1

FS
type: SiteQuality
SIO_000300: 5.149e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.587301587301587e-4
allele num: 6300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -3.839e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.401025e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

QD
type: SiteQuality
SIO_000300: 3.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.25e-1

GenotypeQuality
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bin: 7.5e0
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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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14304
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.37e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.134e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.554e0

DP
type: SiteQuality
SIO_000300: 1.406458e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

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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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546933976857868e-5
allele num: 64644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0489e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 3.204e1

DP
type: SiteQuality
SIO_000300: 1.410469e6

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-2

GenotypeQuality
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bin: 3.25e1
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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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
all individuals: 510
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544830995489093e-5
allele num: 64732
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.582278481012658e-4
allele num: 6320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

QD
type: SiteQuality
SIO_000300: 6.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

FS
type: SiteQuality
SIO_000300: 2.711e0

MQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.334e-1

DP
type: SiteQuality
SIO_000300: 1.415807e6

GenotypeQuality
all individuals: 637
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 293
bin: 5.75e1
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GenotypeQuality
all individuals: 2681
bin: 2.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4999
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.758705592683785e-4
allele num: 11372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64978
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.210000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.141e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -8.735000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.324e0

MQRankSum
type: SiteQuality
SIO_000300: -1.169e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.423434e6

GenotypeQuality
all individuals: 111
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 592
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GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.615506747816882e-5
allele num: 15116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

FS
type: SiteQuality
SIO_000300: 1.3366e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

DP
type: SiteQuality
SIO_000300: 1.426283e6

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.904e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e0

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 354
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variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535720867375146e-5
allele num: 65116
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.131e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

DP
type: SiteQuality
SIO_000300: 1.430094e6

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1004
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GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 2306
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GenotypeQuality
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GenotypeQuality
all individuals: 769
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GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 1720
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variant carriers: 0

GenotypeQuality
all individuals: 748
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variant carriers: 0

GenotypeQuality
all individuals: 729
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GenotypeQuality
all individuals: 916
bin: 3.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.087246921310791e-4
allele num: 9582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533742331288344e-5
allele num: 65200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 9.56e-1

DP
type: SiteQuality
SIO_000300: 1.439369e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

QD
type: SiteQuality
SIO_000300: 1.151e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 4850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
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variant carriers: 0

GenotypeQuality
all individuals: 785
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variant carriers: 1

GenotypeQuality
all individuals: 2257
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GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 737
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GenotypeQuality
all individuals: 55
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 111
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GenotypeQuality
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GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 326
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variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532426137060194e-5
allele num: 65256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.021000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: -7.102000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.69e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.637e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.183e0

DP
type: SiteQuality
SIO_000300: 1.440653e6

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
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GenotypeQuality
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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: 793
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.116020916791536e-5
allele num: 65402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.285948094458733e-3
allele num: 8554
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.89729319504174e-4
allele num: 15812
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.213e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

DP
type: SiteQuality
SIO_000300: 1.446611e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

GenotypeQuality
all individuals: 748
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 316
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GenotypeQuality
all individuals: 790
bin: 9.75e1
variant carriers: 6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15850
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.244796003330558e-4
allele num: 9608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.44777e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

FS
type: SiteQuality
SIO_000300: 4.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

QD
type: SiteQuality
SIO_000300: 1.207e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1961
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GenotypeQuality
all individuals: 610
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526810797605961e-5
allele num: 65496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

MQ
type: SiteQuality
SIO_000300: 4.97e1

FS
type: SiteQuality
SIO_000300: 1.0409e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: -1.628e0

DP
type: SiteQuality
SIO_000300: 1.449041e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.551e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 1026
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 4959
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GenotypeQuality
all individuals: 1936
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variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 2
allele frequency: 1.25328988595062e-4
allele num: 15958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65494
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.039068994181214e-4
allele num: 9624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.606e1

FS
type: SiteQuality
SIO_000300: 2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

DP
type: SiteQuality
SIO_000300: 1.451217e6

VQSLOD
type: SiteQuality
SIO_000300: -5.319e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526065193505067e-5
allele num: 65528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

FS
type: SiteQuality
SIO_000300: 8.272e0

QD
type: SiteQuality
SIO_000300: 1.542e1

VQSLOD
type: SiteQuality
SIO_000300: -1.211e0

MQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

MQ
type: SiteQuality
SIO_000300: 5.78e1

DP
type: SiteQuality
SIO_000300: 1.450859e6

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1001
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526717557251908e-5
allele num: 65500
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

DP
type: SiteQuality
SIO_000300: 1.44633e6

QD
type: SiteQuality
SIO_000300: 1.54e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

FS
type: SiteQuality
SIO_000300: 6.769e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44978
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variant carriers: 0

GenotypeQuality
all individuals: 1919
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4569
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.169272461955389e-4
allele num: 9594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.49e0

DP
type: SiteQuality
SIO_000300: 1.444176e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeQuality
all individuals: 1929
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 9.75e1
variant carriers: 22

East Asian
type: Population
allele count: 6
allele frequency: 7.019185774450163e-4
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.983642578125e-4
allele num: 65536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.041449697979588e-4
allele num: 9602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.750087504375219e-4
allele num: 11428
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.495e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

FS
type: SiteQuality
SIO_000300: 2.446e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

DP
type: SiteQuality
SIO_000300: 1.443459e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

GenotypeQuality
all individuals: 829
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46830
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.170554115759595e-5
allele num: 16206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.154e0

MQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.825e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.13e-1

DP
type: SiteQuality
SIO_000300: 1.447481e6

FS
type: SiteQuality
SIO_000300: 1.446e0

MQ
type: SiteQuality
SIO_000300: 5.764e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.064e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 761
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.569966182250251e-5
allele num: 65646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.514e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

FS
type: SiteQuality
SIO_000300: 5.075e0

DP
type: SiteQuality
SIO_000300: 1.453944e6

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

GenotypeQuality
all individuals: 775
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 85
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65588
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.524e0

DP
type: SiteQuality
SIO_000300: 1.453232e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

GenotypeQuality
all individuals: 93
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 8.75e1
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GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 2.25e1
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GenotypeQuality
all individuals: 558
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.25e1
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GenotypeQuality
all individuals: 4374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 9.75e1
variant carriers: 192

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.4727017629476e-4
allele num: 65572
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.662001399580126e-3
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 122
allele frequency: 1.268718801996672e-2
allele num: 9616
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.473716759431045e-4
allele num: 16170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.229e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

DP
type: SiteQuality
SIO_000300: 1.457914e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.5e0
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GenotypeQuality
all individuals: 614
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 773
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65510
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.336994624912363e-4
allele num: 8558
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.453376e6

MQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 2.145e0

QD
type: SiteQuality
SIO_000300: 1.244e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 761
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.632422530911312e-5
allele num: 65510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16130
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.145e0

MQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

DP
type: SiteQuality
SIO_000300: 1.453376e6

QD
type: SiteQuality
SIO_000300: 1.244e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

GenotypeQuality
all individuals: 701
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 748
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46685
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variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.207324643078833e-5
allele num: 16110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526624328285296e-5
allele num: 65504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

FS
type: SiteQuality
SIO_000300: 3.331e0

DP
type: SiteQuality
SIO_000300: 1.453085e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

QD
type: SiteQuality
SIO_000300: 1.03e1

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47248
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variant carriers: 0

GenotypeQuality
all individuals: 671
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variant carriers: 0

GenotypeQuality
all individuals: 350
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variant carriers: 0

GenotypeQuality
all individuals: 559
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variant carriers: 0

GenotypeQuality
all individuals: 566
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GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 1968
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variant carriers: 0

GenotypeQuality
all individuals: 253
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variant carriers: 0

GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 4451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527043948324833e-5
allele num: 65486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.1291e1

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

DP
type: SiteQuality
SIO_000300: 1.454095e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.323e0

VQSLOD
type: SiteQuality
SIO_000300: -1.453e0

GenotypeQuality
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 597
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 419
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variant carriers: 0

GenotypeQuality
all individuals: 880
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 560
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GenotypeQuality
all individuals: 4451
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 253
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 47260
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16086
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 8.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.207e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.445e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.66e-1

DP
type: SiteQuality
SIO_000300: 1.454696e6

GenotypeQuality
all individuals: 1993
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 586
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.042318115488847e-4
allele num: 9594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

DP
type: SiteQuality
SIO_000300: 1.455062e6

MQ
type: SiteQuality
SIO_000300: 5.906e1

FS
type: SiteQuality
SIO_000300: 1.922e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 592
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variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 20
allele frequency: 2.333722287047841e-3
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526717557251908e-5
allele num: 65500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.021e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.455971e6

MQ
type: SiteQuality
SIO_000300: 5.904e1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

QD
type: SiteQuality
SIO_000300: 1.19e1

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48035
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variant carriers: 0

GenotypeQuality
all individuals: 4514
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GenotypeQuality
all individuals: 269
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GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 889
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GenotypeQuality
all individuals: 279
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GenotypeQuality
all individuals: 590
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variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.055114261273371e-5
allele num: 65464
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.255473539346929e-5
allele num: 15986
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.357e0

DP
type: SiteQuality
SIO_000300: 1.455953e6

FS
type: SiteQuality
SIO_000300: 9.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.841e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

GenotypeQuality
all individuals: 474
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4537
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variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
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GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
all individuals: 95
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GenotypeQuality
all individuals: 147
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65434
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.571832756994656e-4
allele num: 6362
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -7.039e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.321e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.364e0

FS
type: SiteQuality
SIO_000300: 9.863e0

DP
type: SiteQuality
SIO_000300: 1.455528e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

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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bin: 3.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533836431682925e-5
allele num: 65196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.448918e6

MQRankSum
type: SiteQuality
SIO_000300: -8.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.459e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 5.859e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.656e1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068802553243724e-5
allele num: 65172
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.624671916010499e-4
allele num: 11430
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.050420168067227e-4
allele num: 9520
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.212e0

QD
type: SiteQuality
SIO_000300: 1.334e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.450555e6

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534260026389273e-5
allele num: 65178
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.45059e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.107e1

VQSLOD
type: SiteQuality
SIO_000300: -2.039e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

FS
type: SiteQuality
SIO_000300: 1.3017e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

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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variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: -1.994e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 1.0181e1

DP
type: SiteQuality
SIO_000300: 1.442748e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.334e0

QD
type: SiteQuality
SIO_000300: 7.91e0

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65008
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15328
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.587301587301587e-4
allele num: 6300
num of homozygotes: 0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.442992e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9432
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

East Asian
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
allele num: 11408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544163063619518e-5
allele num: 64760
num of homozygotes: 0

Other
type: Population
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-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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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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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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East Asian
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allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
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Latino
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European (Non-Finnish)
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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African
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South Asian
type: Population
allele count: 2
allele frequency: 1.593371574251115e-4
allele num: 12552
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620062858438908e-5
allele num: 61726
num of homozygotes: 0

Other
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: 7.64e-1

MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

Latino
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allele frequency: 9.194556822361162e-5
allele num: 10876
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61336
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQ
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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Latino
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allele frequency: 0.0e0
allele num: 10490
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.683898561950628e-5
allele num: 59386
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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InbreedingCoeff
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DP
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ReadPosRankSum
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SIO_000300: 1.21e0

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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South Asian
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allele frequency: 0.0e0
allele num: 11298
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European (Finnish)
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allele frequency: 0.0e0
allele num: 5586
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8028
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: 1.683898561950628e-5
allele num: 59386
num of homozygotes: 0

African
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allele frequency: 0.0e0
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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DP
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7924
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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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European (Non-Finnish)
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allele count: 2
allele frequency: 3.411106562969027e-5
allele num: 58632
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.148983e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10754
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5484
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.423719528896193e-5
allele num: 58416
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 9.416195856873823e-5
allele num: 10620
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5440
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58108
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.138e0

InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

European (Finnish)
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allele frequency: 0.0e0
allele num: 5440
num of homozygotes: 0

East Asian
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African
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South Asian
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Other
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10178
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 58108
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 57888
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Latino
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European (Finnish)
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South Asian
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African
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Other
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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QD
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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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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African
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allele num: 7964
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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