X-10106933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106933
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106933
    reference: chr 0
allele count: 3
allele frequency: 3.925108921772579e-5
allele num: 76431
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3041G>A
  hgvsp: ENSP00000399584.1:p.Arg1014Gln
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3041G>A
  hgvsp: ENSP00000370242.4:p.Arg1014Gln
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg1014Gln
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7050
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-10106934-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106934
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106934
    reference: chr 0
allele count: 2
allele frequency: 2.614515791675382e-5
allele num: 76496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3042G>T
  hgvsp: ENST00000454666.1:c.3042G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3042G>T
  hgvsp: ENST00000380861.4:c.3042G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg1014Arg
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8879
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

X-10106937-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106937
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106937
    reference: chr 0
allele count: 1
allele frequency: 1.342011675501577e-5
allele num: 74515
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3045C>T
  hgvsp: ENST00000380861.4:c.3045C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3045C>T
  hgvsp: ENST00000454666.1:c.3045C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asp1015Asp
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.464146666009561e-5
  allele num: 40582
  num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-10106941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106941
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106941
    reference: chr 0
allele count: 2
allele frequency: 2.713888323495488e-5
allele num: 73695
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3049C>T
  hgvsp: ENSP00000370242.4:p.Arg1017Trp
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3049C>T
  hgvsp: ENSP00000399584.1:p.Arg1017Trp
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg1017Trp
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 498
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

X-10106944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106944
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106944
    reference: chr 0
allele count: 2
allele frequency: 2.763003384679146e-5
allele num: 72385
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3052C>T
  hgvsp: ENSP00000399584.1:p.Leu1018Phe
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3052C>T
  hgvsp: ENSP00000370242.4:p.Leu1018Phe
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2351
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 48
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  variant carriers: 0
hgvs: p.Leu1018Phe
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8487
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

X-10106948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106948
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106948
    reference: chr 0
allele count: 74
allele frequency: 1.049704947798457e-3
allele num: 70496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3056G>A
  hgvsp: ENSP00000399584.1:p.Arg1019His
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3056G>A
  hgvsp: ENSP00000370242.4:p.Arg1019His
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg1019His
num of homozygotes: 1
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.235635734585444e-4
  allele num: 8093
  num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

X-10106952-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106952
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106952
    reference: chr 0
allele count: 1
allele frequency: 1.444272736463554e-5
allele num: 69239
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3060C>G
  hgvsp: ENST00000454666.1:c.3060C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3060C>G
  hgvsp: ENST00000380861.4:c.3060C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gly1020Gly
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7918
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-10106953-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106953
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106953
    reference: chr 0
allele count: 8
allele frequency: 1.162807598947659e-4
allele num: 68799
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3061C>A
  hgvsp: ENSP00000399584.1:p.Leu1021Met
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3061C>A
  hgvsp: ENSP00000370242.4:p.Leu1021Met
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Leu1021Met
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 7
  allele frequency: 1.870907390084191e-4
  allele num: 37415
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

X-10106958-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106958
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106958
    reference: chr 0
allele count: 2
allele frequency: 3.105879429760537e-5
allele num: 64394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3066G>A
  hgvsp: ENST00000380861.4:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3066G>A
  hgvsp: ENST00000454666.1:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu1022Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 2796
  num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
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X-10106959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106959
    reference: chr 0
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    type: ExactPosition
    position: 24010106959
    reference: chr 0
allele count: 1
allele frequency: 1.560841605793844e-5
allele num: 64068
alternate allele: T
annotation: Annotation
  canonical: false
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  gene symbol: WWC3
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  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
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  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3067C>T
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  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg1023Trp
num of homozygotes: 0
population: European (Non-Finnish)
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  allele num: 34845
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population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
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site quality: ReadPosRankSum
site quality: MQ
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X-10106960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106960
    reference: chr 0
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    type: ExactPosition
    position: 24010106960
    reference: chr 0
allele count: 2
allele frequency: 3.176720988595572e-5
allele num: 62958
alternate allele: A
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000047644
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  gene symbol: WWC3
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  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
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  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
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hgvs: p.Arg1023Gln
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population: African
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population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
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site quality: DP
site quality: FS
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site quality: QD

X-10106967-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106967
    reference: chr 0
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    type: ExactPosition
    position: 24010106967
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 57145
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
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  gene symbol: WWC3
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  hgvsp: ENST00000380861.4:c.3075C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
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  variant of: http://identifiers.org/hgnc/29237
canonical: true
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filter: AC_Adj0_Filter
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genotype depth: GenotypeDepth
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hgvs: p.Ala1025Ala
num of homozygotes: 0
population: Other
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  allele num: 368
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population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
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population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
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site quality: InbreedingCoeff
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X-10106971-C-A
type: Variant
location: Region
  begin: Position
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    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106971
    reference: chr 0
allele count: 1
allele frequency: 1.890966851351096e-5
allele num: 52883
alternate allele: A
annotation: Annotation
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  consequence: synonymous_variant
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  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
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  hgvsp: ENST00000454666.1:c.3079C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
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  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
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  variant of: http://identifiers.org/hgnc/29237
canonical: true
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  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1145
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genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg1027Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6608
  num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

X-10106971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106971
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106971
    reference: chr 0
allele count: 10
allele frequency: 1.890966851351096e-4
allele num: 52883
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3079C>T
  hgvsp: ENSP00000370242.4:p.Arg1027Trp
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3079C>T
  hgvsp: ENSP00000399584.1:p.Arg1027Trp
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg1027Trp
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4292
  num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

X-10106978-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106978
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106978
    reference: chr 0
allele count: 28
allele frequency: 6.412605349945035e-4
allele num: 43664
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+2T>G
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+2T>G
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 26
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hgvs: c.3084+2T>G
num of homozygotes: 0
population: African
  type: Population
  allele count: 5
  allele frequency: 1.29366106080207e-3
  allele num: 3865
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

X-10106978-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106978
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106979
    reference: chr 0
allele count: 1
allele frequency: 2.290216196408941e-5
allele num: 43664
alternate allele: TG
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+7dupG
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+7dupG
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.3084+7dupG
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1515
  num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-10106985-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010106985
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010106985
    reference: chr 0
allele count: 25
allele frequency: 6.190723819428967e-4
allele num: 40383
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+9C>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+9C>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21209
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  variant carriers: 3
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2591
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genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 19
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 22142
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

X-10107002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107002
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107002
    reference: chr 0
allele count: 2
allele frequency: 6.707133035983769e-5
allele num: 29819
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+26C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+26C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3197
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

X-10107003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107003
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107003
    reference: chr 0
allele count: 2
allele frequency: 6.836438215689625e-5
allele num: 29255
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+27G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+27G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3112
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-10107014-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107014
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107014
    reference: chr 0
allele count: 3
allele frequency: 1.184506652979034e-4
allele num: 25327
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+38A>G
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+38A>G
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
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  allele num: 2595
  num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

X-10107020-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107020
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107020
    reference: chr 0
allele count: 1
allele frequency: 4.322455154527772e-5
allele num: 23135
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3084+44C>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3084+44C>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele num: 761
  num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

X-10107403-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107403
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107404
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 21744
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-50_3085-49insG
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-50_3085-49insG
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1734
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

X-10107404-A-AAAAAAAAAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107404
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
allele count: 4
allele frequency: 1.706557446990059e-4
allele num: 23439
alternate allele: AAAAAAAAAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 3
  allele frequency: 1.833516685001834e-4
  allele num: 16362
  num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

X-10107405-A-AAAAAAAAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107405
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
allele count: 1
allele frequency: 4.181650915781551e-5
allele num: 23914
alternate allele: AAAAAAAAT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 631
  num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-10107406-A-AAAAAAAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107406
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
allele count: 1
allele frequency: 3.583458754389737e-5
allele num: 27906
alternate allele: AAAAAAAT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-46_3085-40dupAAAAAAT
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-46_3085-40dupAAAAAAT
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 18407
  num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

X-10107411-A-AAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107411
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
allele count: 1
allele frequency: 2.028685614590307e-5
allele num: 49293
alternate allele: AAT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-41_3085-40dupAT
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-41_3085-40dupAT
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3054
  num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-10107412-ATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107412
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107410
    reference: chr 0
allele count: 1834
allele frequency: 3.928204249485949e-2
allele num: 46688
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-40_3085-39delTC
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-40_3085-39delTC
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 15850
  bin: 1.25e1
  variant carriers: 444
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 434
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 35
genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 17
  allele frequency: 5.29595015576324e-2
  allele num: 321
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: ATC
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

X-10107412-ATCAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107412
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107407
    reference: chr 0
allele count: 1590
allele frequency: 3.405586017820425e-2
allele num: 46688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-40_3085-36delTCAAT
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-40_3085-36delTCAAT
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 483
genotype depth: GenotypeDepth
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  variant carriers: 366
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 126
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 248
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  variant carriers: 92
genotype quality: GenotypeQuality
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  variant carriers: 85
genotype quality: GenotypeQuality
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  variant carriers: 82
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 1417
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 358
  allele frequency: 6.686589465819948e-2
  allele num: 5354
  num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: ATCAAT
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

X-10107413-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
allele count: 168
allele frequency: 1.308207444323314e-2
allele num: 12842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-40T>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-40T>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 2
  allele frequency: 3.1201248049922e-3
  allele num: 641
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum

X-10107414-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
allele count: 251
allele frequency: 1.697896232158561e-2
allele num: 14783
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-39C>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-39C>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2638
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  variant carriers: 34
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 72
genotype depth: GenotypeDepth
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  variant carriers: 32
genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 354
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  variant carriers: 6
genotype quality: GenotypeQuality
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  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1264
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  variant carriers: 3
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 30979
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 487
  bin: 9.75e1
  variant carriers: 264
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 6550
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.25e1
  variant carriers: 5
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 36
  allele frequency: 6.857142857142857e-2
  allele num: 525
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

X-10107414-C-CAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107419
    reference: chr 0
allele count: 56
allele frequency: 3.788135019955354e-3
allele num: 14783
alternate allele: CAAAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-37_3085-36insAAAAA
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-37_3085-36insAAAAA
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
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  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 3384
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genotype depth: GenotypeDepth
  all individuals: 348
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genotype depth: GenotypeDepth
  all individuals: 8535
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  variant carriers: 15
genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 51
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 735
  num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

X-10107414-C-CAAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107420
    reference: chr 0
allele count: 39
allele frequency: 2.63816546032605e-3
allele num: 14783
alternate allele: CAAAAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-37_3085-36insAAAAAA
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-37_3085-36insAAAAAA
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 121
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  variant carriers: 3
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30979
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 888
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
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  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.904761904761905e-3
  allele num: 525
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-10107414-C-CAAAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107421
    reference: chr 0
allele count: 14
allele frequency: 9.470337549888385e-4
allele num: 14783
alternate allele: CAAAAAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-37_3085-36insAAAAAAA
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-37_3085-36insAAAAAAA
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 721
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 487
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  variant carriers: 18
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 8.460236886632825e-4
  allele num: 1182
  num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

X-10107414-C-CAAAAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107422
    reference: chr 0
allele count: 4
allele frequency: 2.705810728539539e-4
allele num: 14783
alternate allele: CAAAAAAAA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 4
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 72
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-10107414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107414
    reference: chr 0
allele count: 2
allele frequency: 1.352905364269769e-4
allele num: 14783
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-39C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-39C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 735
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-10107415-AAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107415
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107413
    reference: chr 0
allele count: 1
allele frequency: 1.914461844775434e-5
allele num: 52234
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-36_3085-35delTA
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-36_3085-35delTA
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12832
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 333
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: AAT
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

X-10107416-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107416
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107415
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 63081
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-36delT
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-36delT
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6383
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: AT
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

X-10107417-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107417
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107417
    reference: chr 0
allele count: 2013
allele frequency: 7.609722904774506e-2
allele num: 26453
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-36T>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-36T>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.75e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 264
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 441
genotype quality: GenotypeQuality
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  variant carriers: 2359
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 367
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  variant carriers: 36
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 35
  allele frequency: 2.470007057163021e-2
  allele num: 1417
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

X-10107424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107424
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107424
    reference: chr 0
allele count: 128
allele frequency: 1.837918557233933e-3
allele num: 69644
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-29G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-29G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 104
num of homozygotes: 1
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5319
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

X-10107424-GTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107424
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107422
    reference: chr 0
allele count: 1
allele frequency: 1.43587387283901e-5
allele num: 69644
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-27_3085-26delCT
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-27_3085-26delCT
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7121
  num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: GTC
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

X-10107426-C-CTTGTTGGTCCAACG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107426
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107440
    reference: chr 0
allele count: 1
allele frequency: 1.29826292420741e-5
allele num: 77026
alternate allele: CTTGTTGGTCCAACG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 521
  num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

X-10107439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107439
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107439
    reference: chr 0
allele count: 29
allele frequency: 3.509281444371839e-4
allele num: 82638
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-14C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-14C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9119
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

X-10107449-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107449
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107449
    reference: chr 0
allele count: 2
allele frequency: 2.372901465266655e-5
allele num: 84285
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3085-4C>G
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3085-4C>G
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.75e1
  variant carriers: 0
hgvs: c.3085-4C>G
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 2
  allele frequency: 2.169197396963124e-4
  allele num: 9220
  num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

X-10107457-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107457
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107457
    reference: chr 0
allele count: 5
allele frequency: 5.871438972263322e-5
allele num: 85158
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3089G>C
  hgvsp: ENSP00000370242.4:p.Arg1030Thr
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3089G>C
  hgvsp: ENSP00000399584.1:p.Arg1030Thr
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2822
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  variant carriers: 0
hgvs: p.Arg1030Thr
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9256
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-10107465-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107465
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107465
    reference: chr 0
allele count: 1
allele frequency: 1.162182578883143e-5
allele num: 86045
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3097A>G
  hgvsp: ENSP00000370242.4:p.Lys1033Glu
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3097A>G
  hgvsp: ENSP00000399584.1:p.Lys1033Glu
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Lys1033Glu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4521
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

X-10107477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107477
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107477
    reference: chr 0
allele count: 3
allele frequency: 3.46008788623231e-5
allele num: 86703
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3109C>T
  hgvsp: ENSP00000399584.1:p.Arg1037Cys
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3109C>T
  hgvsp: ENSP00000370242.4:p.Arg1037Cys
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg1037Cys
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6629
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum

X-10107478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107478
    reference: chr 0
allele count: 14
allele frequency: 1.613646841862609e-4
allele num: 86760
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3110G>A
  hgvsp: ENSP00000370242.4:p.Arg1037His
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3110G>A
  hgvsp: ENSP00000399584.1:p.Arg1037His
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1037His
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 3
  allele frequency: 4.524204494043131e-4
  allele num: 6631
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-10107481-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107481
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107481
    reference: chr 0
allele count: 2
allele frequency: 2.301575428380727e-5
allele num: 86897
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3113A>G
  hgvsp: ENSP00000370242.4:p.His1038Arg
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3113A>G
  hgvsp: ENSP00000399584.1:p.His1038Arg
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.His1038Arg
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8487
  num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

X-10107490-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107490
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107490
    reference: chr 0
allele count: 1
allele frequency: 1.148527587632655e-5
allele num: 87068
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3122C>A
  hgvsp: ENSP00000370242.4:p.Ala1041Glu
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3122C>A
  hgvsp: ENSP00000399584.1:p.Ala1041Glu
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ala1041Glu
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.093101138647019e-5
  allele num: 47776
  num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

X-10107490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107490
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107490
    reference: chr 0
allele count: 1
allele frequency: 1.148527587632655e-5
allele num: 87068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3122C>T
  hgvsp: ENSP00000399584.1:p.Ala1041Val
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3122C>T
  hgvsp: ENSP00000370242.4:p.Ala1041Val
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2106
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ala1041Val
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9704
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

X-10107520-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107520
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107520
    reference: chr 0
allele count: 1
allele frequency: 1.143458275207538e-5
allele num: 87454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3152A>G
  hgvsp: ENSP00000399584.1:p.Lys1051Arg
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3152A>G
  hgvsp: ENSP00000370242.4:p.Lys1051Arg
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
hgvs: p.Lys1051Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9315
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

X-10107524-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107524
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107524
    reference: chr 0
allele count: 1
allele frequency: 1.143419051648239e-5
allele num: 87457
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3156G>C
  hgvsp: ENSP00000370242.4:p.Glu1052Asp
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3156G>C
  hgvsp: ENSP00000399584.1:p.Glu1052Asp
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12317
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 390
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8866
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32585
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu1052Asp
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4530
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

X-10107526-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107526
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107526
    reference: chr 0
allele count: 6
allele frequency: 6.860906554452728e-5
allele num: 87452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3158T>C
  hgvsp: ENSP00000399584.1:p.Ile1053Thr
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3158T>C
  hgvsp: ENSP00000370242.4:p.Ile1053Thr
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 675
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3749
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5520
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 32555
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3197
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genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile1053Thr
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 6
  allele frequency: 1.252661906551422e-4
  allele num: 47898
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

X-10107534-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107534
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107534
    reference: chr 0
allele count: 1
allele frequency: 1.143523653786779e-5
allele num: 87449
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3166C>A
  hgvsp: ENSP00000370242.4:p.Leu1056Met
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3166C>A
  hgvsp: ENSP00000399584.1:p.Leu1056Met
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu1056Met
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.176055509820064e-4
  allele num: 8503
  num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

X-10107537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107537
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107537
    reference: chr 0
allele count: 2
allele frequency: 2.287256550130945e-5
allele num: 87441
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3169C>T
  hgvsp: ENSP00000399584.1:p.Arg1057Cys
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3169C>T
  hgvsp: ENSP00000370242.4:p.Arg1057Cys
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg1057Cys
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 630
  num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

X-10107542-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107542
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107542
    reference: chr 0
allele count: 1
allele frequency: 1.143994600345486e-5
allele num: 87413
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3174G>T
  hgvsp: ENST00000454666.1:c.3174G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3174G>T
  hgvsp: ENST00000380861.4:c.3174G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 248
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3196
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly1058Gly
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6634
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

X-10107572-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107572
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107572
    reference: chr 0
allele count: 3
allele frequency: 3.453793992700982e-5
allele num: 86861
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3204G>C
  hgvsp: ENSP00000370242.4:p.Gln1068His
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3204G>C
  hgvsp: ENSP00000399584.1:p.Gln1068His
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Gln1068His
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 3
  allele frequency: 6.284696763381167e-5
  allele num: 47735
  num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

X-10107587-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107587
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107587
    reference: chr 0
allele count: 1
allele frequency: 1.160038977309638e-5
allele num: 86204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+7C>G
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+7C>G
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.3212+7C>G
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.178411501296253e-4
  allele num: 8486
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-10107587-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107587
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107587
    reference: chr 0
allele count: 6
allele frequency: 6.960233863857825e-5
allele num: 86204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+7C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+7C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.3212+7C>T
num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 2.356823002592505e-4
  allele num: 8486
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-10107593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107593
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107593
    reference: chr 0
allele count: 3
allele frequency: 3.488656053399696e-5
allele num: 85993
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+13C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+13C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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population: European (Finnish)
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population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
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X-10107594-G-A
type: Variant
location: Region
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    reference: chr 0
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    position: 24010107594
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allele count: 3
allele frequency: 3.487682667379704e-5
allele num: 86017
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
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  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+14G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+14G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: European (Finnish)
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  allele num: 4528
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population: Other
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population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
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site quality: DP
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X-10107596-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107596
    reference: chr 0
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    type: ExactPosition
    position: 24010107596
    reference: chr 0
allele count: 1
allele frequency: 1.164374788957069e-5
allele num: 85883
alternate allele: C
annotation: Annotation
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  ensembl protein: ENSP00000399584
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  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+16G>C
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+16G>C
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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population: Other
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population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
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site quality: QD
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X-10107600-AGGCCGGCCCCTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107600
    reference: chr 0
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    position: 24010107588
    reference: chr 0
allele count: 2
allele frequency: 2.330676362280334e-5
allele num: 85812
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
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population: Other
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population: East Asian
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reference allele: AGGCCGGCCCCTC
site quality: QD
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X-10107602-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107602
    reference: chr 0
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    position: 24010107602
    reference: chr 0
allele count: 1
allele frequency: 1.166207958203107e-5
allele num: 85748
alternate allele: C
annotation: Annotation
  canonical: false
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  gene symbol: WWC3
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  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000047644
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  gene symbol: WWC3
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  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4527
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

X-10107603-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107603
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107603
    reference: chr 0
allele count: 1
allele frequency: 1.168142419923837e-5
allele num: 85606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+23C>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+23C>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47404
  num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

X-10107604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107604
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107604
    reference: chr 0
allele count: 8
allele frequency: 9.364501515878683e-5
allele num: 85429
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+24C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+24C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
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  allele frequency: 0.0e0
  allele num: 618
  num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

X-10107605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107605
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107605
    reference: chr 0
allele count: 2
allele frequency: 2.341372044017794e-5
allele num: 85420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+25G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+25G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 47340
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

X-10107612-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107612
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107612
    reference: chr 0
allele count: 1
allele frequency: 1.173832916622648e-5
allele num: 85191
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+32C>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+32C>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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population: European (Non-Finnish)
  type: Population
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  allele num: 47273
  num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-10107612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107612
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107612
    reference: chr 0
allele count: 3
allele frequency: 3.521498749867944e-5
allele num: 85191
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+32C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+32C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 250
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8459
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

X-10107613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107613
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107613
    reference: chr 0
allele count: 2
allele frequency: 2.348410126344465e-5
allele num: 85164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+33G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+33G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 2.363507445048452e-4
  allele num: 8462
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

X-10107619-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107619
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107619
    reference: chr 0
allele count: 2
allele frequency: 2.352470682334121e-5
allele num: 85017
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+39G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+39G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8282
  num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-10107624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107624
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107624
    reference: chr 0
allele count: 17
allele frequency: 2.002332128007915e-4
allele num: 84901
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+44C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+44C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.076889941847943e-4
  allele num: 9286
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

X-10107625-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107625
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107624
    reference: chr 0
allele count: 1
allele frequency: 1.178550383028874e-5
allele num: 84850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+47delC
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+47delC
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
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  allele num: 6623
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: TC
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-10107631-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107631
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107631
    reference: chr 0
allele count: 1
allele frequency: 1.18199118234578e-5
allele num: 84603
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+51C>G
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+51C>G
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
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  allele num: 611
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population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
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site quality: InbreedingCoeff
site quality: BaseQRankSum
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site quality: VQSLOD
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X-10107632-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010107632
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010107632
    reference: chr 0
allele count: 5
allele frequency: 5.910584675036055e-5
allele num: 84594
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3212+52T>C
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3212+52T>C
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  allele num: 9282
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population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
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X-10109429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010109429
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010109429
    reference: chr 0
allele count: 2
allele frequency: 2.363172322525759e-5
allele num: 84632
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3213-46C>T
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3213-46C>T
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  type: Population
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population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
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site quality: MQ
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site quality: DP
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X-10109430-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010109430
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010109430
    reference: chr 0
allele count: 2
allele frequency: 2.359687105489812e-5
allele num: 84757
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000399584
  ensembl transcript: ENST00000454666
  gene symbol: WWC3
  hgvsc: ENST00000454666.1:c.3213-45G>A
  variant of: http://identifiers.org/hgnc/29237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3213-45G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3075
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1860
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 161
  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5207
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 6187
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 3413
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 21247
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 1671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9432
  num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-10109432-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24010109432
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24010109432
    reference: chr 0
allele count: 1
allele frequency: 1.177925672890041e-5
allele num: 84895
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047644
  ensembl protein: ENSP00000370242
  ensembl transcript: ENST00000380861
  gene symbol: WWC3
  hgvsc: ENST00000380861.4:c.3213-43G>A
  variant of: http://identifiers.org/hgnc/29237
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.796163069544364e-5
allele num: 41700
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.141682840506907e-4
allele num: 8759
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6089
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 515
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.107e0

MQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e-1

QD
type: SiteQuality
SIO_000300: 2.268e1

DP
type: SiteQuality
SIO_000300: 1.179609e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7061
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8763
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.79191125380358e-5
allele num: 41737
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.047e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 2.239e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 1.17809e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8643
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 507
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8641
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.351e-1

QD
type: SiteQuality
SIO_000300: 2.787e1

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

DP
type: SiteQuality
SIO_000300: 1.130283e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3283
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.480823337775803e-4
allele num: 6753
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5933
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40127
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.29e0

DP
type: SiteQuality
SIO_000300: 1.110339e6

FS
type: SiteQuality
SIO_000300: 2.966e0

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: -5.087e-1

African
type: Population
allele count: 2
allele frequency: 3.027550711474417e-4
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39389
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8335
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.445e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

FS
type: SiteQuality
SIO_000300: 1.627e0

DP
type: SiteQuality
SIO_000300: 1.071083e6

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.22e0

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

Other
type: Population
allele count: 1
allele frequency: 2.11864406779661e-3
allele num: 472
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.124511795032026e-4
allele num: 6401
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5744
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 9.586578789694428e-4
allele num: 8345
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 62
allele frequency: 1.617067890769672e-3
allele num: 38341
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 1.030552e6

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

QD
type: SiteQuality
SIO_000300: 1.66e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.18e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 6.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.161e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37666
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.592863969417012e-4
allele num: 6278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3013
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5661
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 461
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-3

DP
type: SiteQuality
SIO_000300: 9.99284e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.77e0

QD
type: SiteQuality
SIO_000300: 1.544e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6241
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.346720214190094e-4
allele num: 2988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8195
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.196e0

FS
type: SiteQuality
SIO_000300: 1.1338e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.12e-1

QD
type: SiteQuality
SIO_000300: 1.481e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

DP
type: SiteQuality
SIO_000300: 9.88773e5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5809
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5299
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34997
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 417
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7295
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.570363706464465e-4
allele num: 7781
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

QD
type: SiteQuality
SIO_000300: 1.161e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.426e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 8.95626e5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2766
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 415
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5275
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7749
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

FS
type: SiteQuality
SIO_000300: 1.221e0

VQSLOD
type: SiteQuality
SIO_000300: -1.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e-1

DP
type: SiteQuality
SIO_000300: 8.95177e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

QD
type: SiteQuality
SIO_000300: 1.018e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5162
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7658
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2693
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7087
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.92141396435875e-5
allele num: 34230
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 8.71302e5

FS
type: SiteQuality
SIO_000300: 3.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.492e1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4629
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31124
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5196
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2345
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6419
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.67167e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.264e-1

QD
type: SiteQuality
SIO_000300: 2.422e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 335
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4292
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5849
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.088118605136772e-4
allele num: 4789
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28850
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.13e-2

DP
type: SiteQuality
SIO_000300: 7.05819e5

QD
type: SiteQuality
SIO_000300: 1.721e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

African
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allele count: 6
allele frequency: 1.252871163082063e-3
allele num: 4789
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.709693964780304e-4
allele num: 5849
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 3.026634382566586e-4
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.466204506065858e-5
allele num: 28850
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.13e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 1.721e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.05819e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 273
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East Asian
type: Population
allele count: 1
allele frequency: 2.875215641173088e-4
allele num: 3478
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European (Finnish)
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allele frequency: 1.32013201320132e-3
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South Asian
type: Population
allele count: 1
allele frequency: 1.965022597759874e-4
allele num: 5089
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European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 7.958115183246073e-4
allele num: 23875
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Latino
type: Population
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allele frequency: 0.0e0
allele num: 5569
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MQ
type: SiteQuality
SIO_000300: 5.917e1

QD
type: SiteQuality
SIO_000300: 8.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 6.31076e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.72e-2

FS
type: SiteQuality
SIO_000300: 3.28696e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.575e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3865
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5569
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 273
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23875
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.965022597759874e-4
allele num: 5089
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DP
type: SiteQuality
SIO_000300: 6.31076e5

QD
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.72e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.28696e2

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.575e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

East Asian
type: Population
allele count: 0
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allele num: 3201
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Latino
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allele frequency: 4.863813229571985e-3
allele num: 5140
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1432
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African
type: Population
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allele num: 3668
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South Asian
type: Population
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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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.51e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

FS
type: SiteQuality
SIO_000300: 1.3157e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.164e0

VQSLOD
type: SiteQuality
SIO_000300: -1.388e0

DP
type: SiteQuality
SIO_000300: 5.49153e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.497e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 966
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Other
type: Population
allele count: 0
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allele num: 197
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2803
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16601
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Latino
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allele count: 1
allele frequency: 2.642007926023778e-4
allele num: 3785
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East Asian
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allele frequency: 4.405286343612335e-4
allele num: 2270
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 4.51496e5

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.85e-2

FS
type: SiteQuality
SIO_000300: 3.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2260
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 191
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 950
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2754
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3711
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 1.22872765251582e-4
allele num: 16277
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.435e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.92e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.973e-1

DP
type: SiteQuality
SIO_000300: 4.47342e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2443
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 823
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1914
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3134
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QD
type: SiteQuality
SIO_000300: 2.051e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.22e-2

DP
type: SiteQuality
SIO_000300: 4.06757e5

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.288e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1693
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2797
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 155
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13160
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 4.23908435777872e-4
allele num: 2359
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.299e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.098e0

MQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.52e-2

QD
type: SiteQuality
SIO_000300: 8.08e0

DP
type: SiteQuality
SIO_000300: 3.93556e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 481
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 801
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 181
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1973
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.82e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.537e0

DP
type: SiteQuality
SIO_000300: 8.44854e5

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 7.95e0

MQ
type: SiteQuality
SIO_000300: 5.093e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1351
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1988
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European (Finnish)
type: Population
allele count: 1
allele frequency: 4.889975550122249e-4
allele num: 2045
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 189
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.619999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

QD
type: SiteQuality
SIO_000300: 4.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-2

MQ
type: SiteQuality
SIO_000300: 5.863e1

FS
type: SiteQuality
SIO_000300: 1.673e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 8.45501e5

Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
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allele frequency: 0.0e0
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African
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Other
type: Population
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2091
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European (Non-Finnish)
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allele count: 1
allele frequency: 6.116207951070337e-5
allele num: 16350
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MQ
type: SiteQuality
SIO_000300: 5.268e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.54e-2

DP
type: SiteQuality
SIO_000300: 8.48908e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e0

VQSLOD
type: SiteQuality
SIO_000300: -3.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1995
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Other
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allele count: 0
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allele num: 207
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East Asian
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allele num: 1473
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African
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allele frequency: 3.815337657382679e-4
allele num: 2621
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 917
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2286
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQ
type: SiteQuality
SIO_000300: 5.154e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.377e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.886e0

DP
type: SiteQuality
SIO_000300: 8.54608e5

South Asian
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num of homozygotes: 0

African
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Latino
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allele num: 5585
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East Asian
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allele count: 1
allele frequency: 2.555583950932788e-4
allele num: 3913
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 336
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 28243
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.687e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e0

East Asian
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allele frequency: 5.950457727517501e-2
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num of homozygotes: 0

South Asian
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allele frequency: 5.353602115003304e-2
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European (Finnish)
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allele count: 30
allele frequency: 1.183431952662722e-2
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African
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allele frequency: 7.756813417190776e-2
allele num: 5247
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European (Non-Finnish)
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allele count: 630
allele frequency: 2.37816616964252e-2
allele num: 26491
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Latino
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allele count: 367
allele frequency: 6.854688083675757e-2
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
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MQ
type: SiteQuality
SIO_000300: 5.574e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.289e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7242e1

African
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allele frequency: 5.908137983609682e-2
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East Asian
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allele frequency: 5.411954765751212e-2
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Other
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allele frequency: 4.049844236760124e-2
allele num: 321
num of homozygotes: 0

European (Finnish)
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allele count: 42
allele frequency: 1.656804733727811e-2
allele num: 2535
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European (Non-Finnish)
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allele count: 494
allele frequency: 1.864784266354611e-2
allele num: 26491
num of homozygotes: 0

South Asian
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allele frequency: 5.684071381361534e-2
allele num: 3026
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.289e-1

MQ
type: SiteQuality
SIO_000300: 5.574e1

FS
type: SiteQuality
SIO_000300: 1.7242e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e0

QD
type: SiteQuality
SIO_000300: 6.14e0

Latino
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allele frequency: 5.18018018018018e-2
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East Asian
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allele frequency: 6.182795698924731e-2
allele num: 372
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European (Non-Finnish)
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allele count: 71
allele frequency: 6.975144906179389e-3
allele num: 10179
num of homozygotes: 0

Other
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South Asian
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allele count: 16
allele frequency: 4.878048780487805e-2
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African
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allele count: 33
allele frequency: 4.094292803970223e-2
allele num: 806
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.978e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.077e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e0

VQSLOD
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SIO_000300: -3.735e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

MQ
type: SiteQuality
SIO_000300: 5.364e1

FS
type: SiteQuality
SIO_000300: 5.5722e1

DP
type: SiteQuality
SIO_000300: 7.4806e5

MQRankSum
type: SiteQuality
SIO_000300: -1.977e0

European (Non-Finnish)
type: Population
allele count: 123
allele frequency: 1.088014153029633e-2
allele num: 11305
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 8.16326530612245e-3
allele num: 735
num of homozygotes: 0

African
type: Population
allele count: 42
allele frequency: 3.553299492385787e-2
allele num: 1182
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 4.49438202247191e-2
allele num: 445
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

East Asian
type: Population
allele count: 24
allele frequency: 4.624277456647399e-2
allele num: 519
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.413e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

VQSLOD
type: SiteQuality
SIO_000300: -4.831e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.239e0

FS
type: SiteQuality
SIO_000300: 5.1772e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

QD
type: SiteQuality
SIO_000300: 1.312e1

MQ
type: SiteQuality
SIO_000300: 5.38e1

DP
type: SiteQuality
SIO_000300: 7.84235e5

African
type: Population
allele count: 11
allele frequency: 9.306260575296108e-3
allele num: 1182
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 1.573033707865169e-2
allele num: 445
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.388888888888889e-2
allele num: 72
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 2.504816955684008e-2
allele num: 519
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 1.238390092879257e-3
allele num: 11305
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.904761904761905e-2
allele num: 525
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.831e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.239e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.413e-1

DP
type: SiteQuality
SIO_000300: 7.84235e5

FS
type: SiteQuality
SIO_000300: 5.1772e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

MQ
type: SiteQuality
SIO_000300: 5.38e1

European (Finnish)
type: Population
allele count: 4
allele frequency: 5.442176870748299e-3
allele num: 735
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.734104046242774e-2
allele num: 519
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.061477222467935e-3
allele num: 11305
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 7.614213197969543e-3
allele num: 1182
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 8.988764044943821e-3
allele num: 445
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.38e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

VQSLOD
type: SiteQuality
SIO_000300: -4.831e-1

FS
type: SiteQuality
SIO_000300: 5.1772e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

DP
type: SiteQuality
SIO_000300: 7.84235e5

MQRankSum
type: SiteQuality
SIO_000300: -2.239e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.413e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 445
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.80952380952381e-3
allele num: 525
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.348747591522158e-2
allele num: 519
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.360544217687075e-3
allele num: 735
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 2.653693056169837e-4
allele num: 11305
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 7.84235e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.413e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.831e-1

MQ
type: SiteQuality
SIO_000300: 5.38e1

MQRankSum
type: SiteQuality
SIO_000300: -2.239e0

QD
type: SiteQuality
SIO_000300: 1.312e1

FS
type: SiteQuality
SIO_000300: 5.1772e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 525
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 445
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11305
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.692047377326565e-3
allele num: 1182
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.853564547206166e-3
allele num: 519
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 735
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.1772e1

VQSLOD
type: SiteQuality
SIO_000300: -4.831e-1

MQ
type: SiteQuality
SIO_000300: 5.38e1

DP
type: SiteQuality
SIO_000300: 7.84235e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.413e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

MQRankSum
type: SiteQuality
SIO_000300: -2.239e0

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.769128704113224e-4
allele num: 11305
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 525
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 519
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 445
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

QD
type: SiteQuality
SIO_000300: 1.312e1

VQSLOD
type: SiteQuality
SIO_000300: -4.831e-1

DP
type: SiteQuality
SIO_000300: 7.84235e5

MQ
type: SiteQuality
SIO_000300: 5.38e1

MQRankSum
type: SiteQuality
SIO_000300: -2.239e0

FS
type: SiteQuality
SIO_000300: 5.1772e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.413e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5307
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3969
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3387
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.238971302714258e-5
allele num: 30874
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

FS
type: SiteQuality
SIO_000300: 3.269e0

VQSLOD
type: SiteQuality
SIO_000300: -5.663e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.135e0

QD
type: SiteQuality
SIO_000300: 3.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.75e-2

DP
type: SiteQuality
SIO_000300: 9.77285e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.835e0

MQ
type: SiteQuality
SIO_000300: 5.65e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3477
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4693
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36367
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4757
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

QD
type: SiteQuality
SIO_000300: 5.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

DP
type: SiteQuality
SIO_000300: 1.020121e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: -1.336e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

Latino
type: Population
allele count: 398
allele frequency: 2.185612300933553e-1
allele num: 1821
num of homozygotes: 0

African
type: Population
allele count: 437
allele frequency: 1.32786387116378e-1
allele num: 3291
num of homozygotes: 0

East Asian
type: Population
allele count: 233
allele frequency: 1.147218119153127e-1
allele num: 2031
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 743
allele frequency: 4.499485254042269e-2
allele num: 16513
num of homozygotes: 0

South Asian
type: Population
allele count: 153
allele frequency: 1.260296540362438e-1
allele num: 1214
num of homozygotes: 0

Other
type: Population
allele count: 14
allele frequency: 8.433734939759036e-2
allele num: 166
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.8294e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.866e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e0

QD
type: SiteQuality
SIO_000300: 1.065e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.693e0

VQSLOD
type: SiteQuality
SIO_000300: 6.27e0

MQ
type: SiteQuality
SIO_000300: 5.696e1

DP
type: SiteQuality
SIO_000300: 1.073071e6

MQRankSum
type: SiteQuality
SIO_000300: -1.736e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.273e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.027926960257787e-4
allele num: 7448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5033
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40865
num of homozygotes: 0

African
type: Population
allele count: 125
allele frequency: 1.755371436595984e-2
allele num: 7121
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MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

DP
type: SiteQuality
SIO_000300: 1.420603e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

QD
type: SiteQuality
SIO_000300: 1.766e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.447081854888046e-5
allele num: 40865
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5033
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.42e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.766e1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

DP
type: SiteQuality
SIO_000300: 1.420603e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8735
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6209
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8021
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.302927020242729e-5
allele num: 43423
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3397
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

QD
type: SiteQuality
SIO_000300: 4.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.268e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

FS
type: SiteQuality
SIO_000300: 4.288e0

MQ
type: SiteQuality
SIO_000300: 5.865e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

DP
type: SiteQuality
SIO_000300: 1.476462e6

East Asian
type: Population
allele count: 25
allele frequency: 3.826140189776553e-3
allele num: 6534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4383
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.619515389652914e-4
allele num: 7635
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.736111111111111e-3
allele num: 576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.17141120013897e-5
allele num: 46053
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

FS
type: SiteQuality
SIO_000300: 1.278e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.301e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e-1

QD
type: SiteQuality
SIO_000300: 1.655e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.593894e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.832e1

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

DP
type: SiteQuality
SIO_000300: 1.633146e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.626e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8433
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.059366922327217e-4
allele num: 47198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.045e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.254e0

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.042e0

MQ
type: SiteQuality
SIO_000300: 5.902e1

DP
type: SiteQuality
SIO_000300: 1.650276e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 2.537e1

African
type: Population
allele count: 1
allele frequency: 1.181614084839891e-4
allele num: 8463
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9285
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.789e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 1.662646e6

MQRankSum
type: SiteQuality
SIO_000300: -7.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.142e-1

FS
type: SiteQuality
SIO_000300: 4.327e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.292606187729418e-5
allele num: 47675
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8485
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9297
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 1.678192e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.57e-2

FS
type: SiteQuality
SIO_000300: 5.455e0

VQSLOD
type: SiteQuality
SIO_000300: -1.852e0

QD
type: SiteQuality
SIO_000300: 2.401e1

MQ
type: SiteQuality
SIO_000300: 5.893e1

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47691
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8485
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075500107550011e-4
allele num: 9298
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 1.051856526769749e-3
allele num: 9507
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 1.679856e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.56e-2

FS
type: SiteQuality
SIO_000300: 7.797e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.552e1

MQ
type: SiteQuality
SIO_000300: 5.9e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.84e-1

South Asian
type: Population
allele count: 2
allele frequency: 2.085070892410342e-4
allele num: 9592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47731
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

VQSLOD
type: SiteQuality
SIO_000300: -1.317e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.56e-2

QD
type: SiteQuality
SIO_000300: 1.77e1

FS
type: SiteQuality
SIO_000300: 7.474e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

DP
type: SiteQuality
SIO_000300: 1.682064e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8493
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.092e0

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 1.687649e6

MQ
type: SiteQuality
SIO_000300: 5.864e1

QD
type: SiteQuality
SIO_000300: 2.087e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.789e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8493
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093101138647019e-5
allele num: 47776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.687649e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.789e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-2

QD
type: SiteQuality
SIO_000300: 2.087e1

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

MQ
type: SiteQuality
SIO_000300: 5.864e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087726257333138e-5
allele num: 47899
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9941
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8503
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.649e-1

FS
type: SiteQuality
SIO_000300: 4.24e0

QD
type: SiteQuality
SIO_000300: 1.197e1

MQ
type: SiteQuality
SIO_000300: 5.869e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

DP
type: SiteQuality
SIO_000300: 1.697002e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 1.504e1

VQSLOD
type: SiteQuality
SIO_000300: -4.93e-2

MQ
type: SiteQuality
SIO_000300: 5.93e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.697388e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.446e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.188e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9943
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8503
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.697598e6

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.29e-2

QD
type: SiteQuality
SIO_000300: 1.364e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47895
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.913e1

QD
type: SiteQuality
SIO_000300: 1.361e1

DP
type: SiteQuality
SIO_000300: 1.697778e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.265e0

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

FS
type: SiteQuality
SIO_000300: 7.278e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087944210130705e-5
allele num: 47894
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

DP
type: SiteQuality
SIO_000300: 1.697758e6

VQSLOD
type: SiteQuality
SIO_000300: -2.223e-1

FS
type: SiteQuality
SIO_000300: 1.591e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47881
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.008572869389813e-4
allele num: 9915
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9317
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.646e1

VQSLOD
type: SiteQuality
SIO_000300: -4.507e-1

DP
type: SiteQuality
SIO_000300: 1.697133e6

MQ
type: SiteQuality
SIO_000300: 5.787e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.29e-2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6635
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8499
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.165e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

QD
type: SiteQuality
SIO_000300: 1.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.44e-1

FS
type: SiteQuality
SIO_000300: 1.0014e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

DP
type: SiteQuality
SIO_000300: 1.677835e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9075
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6627
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.726e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

FS
type: SiteQuality
SIO_000300: 5.93e-1

MQ
type: SiteQuality
SIO_000300: 5.878e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 1.659291e6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.102695655830775e-5
allele num: 47558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.526935264825713e-4
allele num: 6627
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9075
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.878e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

QD
type: SiteQuality
SIO_000300: 1.726e1

FS
type: SiteQuality
SIO_000300: 5.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.659291e6

MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8932
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.357934449422306e-4
allele num: 8482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.105263157894737e-5
allele num: 47500
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.119e-1

FS
type: SiteQuality
SIO_000300: 7.96e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

DP
type: SiteQuality
SIO_000300: 1.652488e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9305
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.509206157561123e-4
allele num: 6626
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.235885969815539e-4
allele num: 8945
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47511
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.347e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.76e-2

DP
type: SiteQuality
SIO_000300: 1.652004e6

VQSLOD
type: SiteQuality
SIO_000300: -2.041e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

QD
type: SiteQuality
SIO_000300: 2.234e1

MQ
type: SiteQuality
SIO_000300: 5.889e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8479
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8865
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.106726778604083e-5
allele num: 47467
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.64719e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 1.907e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.848e0

QD
type: SiteQuality
SIO_000300: 2.159e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.107170701898561e-5
allele num: 47457
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.135718341851221e-4
allele num: 8805
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

MQ
type: SiteQuality
SIO_000300: 3.744e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: -1.418e0

DP
type: SiteQuality
SIO_000300: 1.645292e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
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East Asian
type: Population
allele count: 1
allele frequency: 1.509433962264151e-4
allele num: 6625
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8771
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47431
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 1.107e0

VQSLOD
type: SiteQuality
SIO_000300: 2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.928e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.97e-1

QD
type: SiteQuality
SIO_000300: 1.077e1

DP
type: SiteQuality
SIO_000300: 1.642957e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8471
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.154467790348649e-4
allele num: 8662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.521e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

DP
type: SiteQuality
SIO_000300: 1.639097e6

VQSLOD
type: SiteQuality
SIO_000300: 7.5e-2

QD
type: SiteQuality
SIO_000300: 2.965e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.903187721369539e-4
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.223954043380008e-5
allele num: 47349
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.888e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.850000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.45e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-1

DP
type: SiteQuality
SIO_000300: 1.63557e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.180916391119509e-4
allele num: 8468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.170823088631308e-4
allele num: 8541
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
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VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.635084e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

QD
type: SiteQuality
SIO_000300: 1.532e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

East Asian
type: Population
allele count: 1
allele frequency: 1.509661835748792e-4
allele num: 6624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8459
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8397
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9297
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

VQSLOD
type: SiteQuality
SIO_000300: 2.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.13e-2

DP
type: SiteQuality
SIO_000300: 1.629791e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

QD
type: SiteQuality
SIO_000300: 1.731e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8397
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47273
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.226847370119393e-4
allele num: 9297
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.629791e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.731e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47261
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.77e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -1.736e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

QD
type: SiteQuality
SIO_000300: 2.777e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 1.628304e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
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allele num: 8449
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East Asian
type: Population
allele count: 2
allele frequency: 3.019779556092405e-4
allele num: 6623
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47230
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.623445e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.405e0

FS
type: SiteQuality
SIO_000300: 3.045e0

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.419e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

Other
type: Population
allele count: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6622
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European (Finnish)
type: Population
allele count: 0
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num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.702541651465402e-3
allele num: 8223
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.238455506813317e-5
allele num: 47187
num of homozygotes: 0

African
type: Population
allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.52e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.45e-1

DP
type: SiteQuality
SIO_000300: 1.620405e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.521e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.319e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

QD
type: SiteQuality
SIO_000300: 2.153e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9287
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47177
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
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allele num: 610
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 5.695e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.407e1

DP
type: SiteQuality
SIO_000300: 1.620286e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.429e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47079
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.858e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.43e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.918e0

DP
type: SiteQuality
SIO_000300: 1.626989e6

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.496176720475786e-5
allele num: 47080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6617
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.24285359184688e-4
allele num: 8046
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.629907e6

FS
type: SiteQuality
SIO_000300: 1.421e0

QD
type: SiteQuality
SIO_000300: 1.908e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.034e0

MQ
type: SiteQuality
SIO_000300: 5.9e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9399
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.097574360662935e-4
allele num: 9111
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.200192030724916e-4
allele num: 8332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.608e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 2.384e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.296e0

DP
type: SiteQuality
SIO_000300: 1.628214e6

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

QD
type: SiteQuality
SIO_000300: 3.047e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9109
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.30737422467264e-5
allele num: 46432
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.632324e6

FS
type: SiteQuality
SIO_000300: 1.295e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.037e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.436e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.851e1