X-73814214-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814214
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814214
    reference: chr 0
allele count: 5
allele frequency: 5.797303094600392e-5
allele num: 86247
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.180T>C
  hgvsp: ENST00000332687.6:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.180T>C
  hgvsp: ENST00000349225.2:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
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  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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  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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  bin: 9.75e1
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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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  variant carriers: 0
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: 5120
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  variant carriers: 0
hgvs: p.Thr60Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4516
  num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

X-73814243-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814243
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814243
    reference: chr 0
allele count: 1
allele frequency: 1.177648236471766e-5
allele num: 84915
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-19C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-19C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
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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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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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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8323
  num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-73814244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814244
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814244
    reference: chr 0
allele count: 1
allele frequency: 1.177481837342659e-5
allele num: 84927
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-20C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-20C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1722
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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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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: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 609
  num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

X-73814251-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814251
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814252
    reference: chr 0
allele count: 1
allele frequency: 1.180790893740627e-5
allele num: 84689
alternate allele: AC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-28_170-27insG
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-28_170-27insG
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.122826756108434e-5
  allele num: 47107
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

X-73814252-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814252
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814252
    reference: chr 0
allele count: 1
allele frequency: 1.181488439135623e-5
allele num: 84639
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-28A>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-28A>G
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
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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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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.123412748970145e-5
  allele num: 47094
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
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site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
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X-73814252-T-TGTGGGATGGTCAGAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814252
    reference: chr 0
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    type: ExactPosition
    position: 24073814267
    reference: chr 0
allele count: 1
allele frequency: 1.181488439135623e-5
allele num: 84639
alternate allele: TGTGGGATGGTCAGAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
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  bin: 8.25e1
  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: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9272
  num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-73814258-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814258
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814258
    reference: chr 0
allele count: 2
allele frequency: 2.371325926892022e-5
allele num: 84341
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-34A>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-34A>G
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
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genotype depth: GenotypeDepth
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  allele num: 7999
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population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

X-73814261-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814261
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814261
    reference: chr 0
allele count: 1
allele frequency: 1.188128222797804e-5
allele num: 84166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-37C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-37C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2695
  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: 2.131332722351286e-5
  allele num: 46919
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-73814263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814263
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814263
    reference: chr 0
allele count: 356
allele frequency: 4.236279689656813e-3
allele num: 84036
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-39C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-39C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 3.25e1
  variant carriers: 41
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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  bin: 3.75e1
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num of homozygotes: 3
population: European (Finnish)
  type: Population
  allele count: 12
  allele frequency: 2.675585284280936e-3
  allele num: 4485
  num of homozygotes: 1
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

X-73814263-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814263
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814263
    reference: chr 0
allele count: 1
allele frequency: 1.189966204959779e-5
allele num: 84036
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-39C>A
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-39C>A
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 8405
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

X-73814270-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814270
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814270
    reference: chr 0
allele count: 1
allele frequency: 1.194785954096324e-5
allele num: 83697
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-46T>C
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-46T>C
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 3.25e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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 frequency: 0.0e0
  allele num: 7725
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

X-73814273-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073814273
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073814273
    reference: chr 0
allele count: 1
allele frequency: 1.199069522050888e-5
allele num: 83398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.170-49G>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.170-49G>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: Other
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  allele num: 593
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population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

X-73815607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815607
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815607
    reference: chr 0
allele count: 1
allele frequency: 1.460728319139923e-5
allele num: 68459
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+37G>A
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+37G>A
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8200
  num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

X-73815613-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815613
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815613
    reference: chr 0
allele count: 4
allele frequency: 5.786283614691374e-5
allele num: 69129
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+31G>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+31G>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 924
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 4.25e1
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2910
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7732
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

X-73815619-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815619
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815619
    reference: chr 0
allele count: 1
allele frequency: 1.427796339130186e-5
allele num: 70038
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+25T>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+25T>G
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.204529029149603e-4
  allele num: 8302
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

X-73815623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815623
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815623
    reference: chr 0
allele count: 1
allele frequency: 1.410357666704276e-5
allele num: 70904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+21G>A
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+21G>A
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5929
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

X-73815629-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815629
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815629
    reference: chr 0
allele count: 2
allele frequency: 2.761744317711066e-5
allele num: 72418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+15A>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+15A>G
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  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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genotype quality: GenotypeQuality
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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: 7935
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

X-73815633-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815633
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815633
    reference: chr 0
allele count: 4
allele frequency: 5.444843732984864e-5
allele num: 73464
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+11A>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
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  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
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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: Latino
  type: Population
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  allele num: 8572
  num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
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X-73815638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815638
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815638
    reference: chr 0
allele count: 4
allele frequency: 5.343307507347048e-5
allele num: 74860
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+6C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+6C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.169+6C>T
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8087
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
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site quality: FS
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site quality: VQSLOD
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X-73815640-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815640
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815640
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 75737
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+4T>C
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+4T>C
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.169+4T>C
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population: East Asian
  type: Population
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  allele num: 6214
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-73815641-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815641
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815641
    reference: chr 0
allele count: 1
allele frequency: 1.315858729406811e-5
allele num: 75996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.169+3A>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.169+3A>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: c.169+3A>T
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
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  allele num: 6224
  num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-73815663-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815663
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815663
    reference: chr 0
allele count: 1
allele frequency: 1.235055824523268e-5
allele num: 80968
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.150C>G
  hgvsp: ENSP00000328059.6:p.Asn50Lys
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.150C>G
  hgvsp: ENSP00000253571.3:p.Asn50Lys
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  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 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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
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  bin: 5.75e1
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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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  bin: 7.75e1
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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
  all individuals: 2911
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn50Lys
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 577
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

X-73815690-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815690
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815690
    reference: chr 0
allele count: 1
allele frequency: 1.190759704691593e-5
allele num: 83980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.123A>G
  hgvsp: ENST00000349225.2:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.123A>G
  hgvsp: ENST00000332687.6:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Glu41Glu
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6499
  num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-73815708-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815708
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815708
    reference: chr 0
allele count: 164
allele frequency: 1.930002118295008e-3
allele num: 84974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.105T>C
  hgvsp: ENST00000349225.2:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.105T>C
  hgvsp: ENST00000332687.6:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
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  variant carriers: 5
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Phe35Phe
num of homozygotes: 0
population: Other
  type: Population
  allele count: 1
  allele frequency: 1.623376623376623e-3
  allele num: 616
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-73815717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815717
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815717
    reference: chr 0
allele count: 1
allele frequency: 1.171028748755782e-5
allele num: 85395
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.96C>T
  hgvsp: ENST00000332687.6:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.96C>T
  hgvsp: ENST00000349225.2:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Phe32Phe
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.149844136300118e-5
  allele num: 46515
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

X-73815729-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815729
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815729
    reference: chr 0
allele count: 1
allele frequency: 1.16293944574306e-5
allele num: 85989
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.84A>C
  hgvsp: ENST00000332687.6:c.84A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.84A>C
  hgvsp: ENST00000349225.2:c.84A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 6.25e1
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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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  bin: 3.75e1
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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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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Arg28Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9232
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS

X-73815747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815747
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815747
    reference: chr 0
allele count: 446
allele frequency: 5.15172166841856e-3
allele num: 86573
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.66G>A
  hgvsp: ENST00000349225.2:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.66G>A
  hgvsp: ENST00000332687.6:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
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  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 424
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genotype depth: GenotypeDepth
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  variant carriers: 25
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 8.75e1
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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: 403
hgvs: p.Gln22Gln
num of homozygotes: 7
population: Latino
  type: Population
  allele count: 32
  allele frequency: 3.457216940363008e-3
  allele num: 9256
  num of homozygotes: 1
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

X-73815756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815756
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815756
    reference: chr 0
allele count: 1
allele frequency: 1.155494956264516e-5
allele num: 86543
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.57C>T
  hgvsp: ENST00000332687.6:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.57C>T
  hgvsp: ENST00000349225.2:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 353
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  variant carriers: 0
hgvs: p.Arg19Arg
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47422
  num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

X-73815757-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815757
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815757
    reference: chr 0
allele count: 1
allele frequency: 1.155548365476837e-5
allele num: 86539
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.56G>T
  hgvsp: ENSP00000253571.3:p.Arg19Leu
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.56G>T
  hgvsp: ENSP00000328059.6:p.Arg19Leu
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg19Leu
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9265
  num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS

X-73815758-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815758
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815758
    reference: chr 0
allele count: 1
allele frequency: 1.155214638879904e-5
allele num: 86564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.55C>T
  hgvsp: ENSP00000253571.3:p.Arg19Cys
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.55C>T
  hgvsp: ENSP00000328059.6:p.Arg19Cys
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg19Cys
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9266
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-73815770-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815770
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815770
    reference: chr 0
allele count: 1
allele frequency: 1.159178374368248e-5
allele num: 86268
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.43T>C
  hgvsp: ENSP00000328059.6:p.Ser15Pro
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.43T>C
  hgvsp: ENSP00000253571.3:p.Ser15Pro
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
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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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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2848
  bin: 9.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5024
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser15Pro
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9270
  num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

X-73815789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815789
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815789
    reference: chr 0
allele count: 1
allele frequency: 1.172951733036186e-5
allele num: 85255
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.24C>T
  hgvsp: ENST00000349225.2:c.24C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.24C>T
  hgvsp: ENST00000332687.6:c.24C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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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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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4046
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp8Asp
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9238
  num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

X-73815793-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815793
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815793
    reference: chr 0
allele count: 1
allele frequency: 1.177551164598102e-5
allele num: 84922
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.20A>G
  hgvsp: ENSP00000328059.6:p.Asn7Ser
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.20A>G
  hgvsp: ENSP00000253571.3:p.Asn7Ser
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.75e1
  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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  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
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4879
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 565
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  variant carriers: 0
hgvs: p.Asn7Ser
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8395
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

X-73815796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815796
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815796
    reference: chr 0
allele count: 7
allele frequency: 8.272764876203983e-5
allele num: 84615
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.17C>T
  hgvsp: ENSP00000328059.6:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.17C>T
  hgvsp: ENSP00000253571.3:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
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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: 1252
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser6Phe
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 6
  allele frequency: 6.899724011039559e-4
  allele num: 8696
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

X-73815806-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815806
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815806
    reference: chr 0
allele count: 1
allele frequency: 1.197647819682144e-5
allele num: 83497
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.7A>G
  hgvsp: ENSP00000253571.3:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.7A>G
  hgvsp: ENSP00000328059.6:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13476
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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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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  variant carriers: 0
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
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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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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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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
  all individuals: 38003
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn3Asp
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.169479758753851e-5
  allele num: 46094
  num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

X-73815816-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815816
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815816
    reference: chr 0
allele count: 2
allele frequency: 2.435371333244036e-5
allele num: 82123
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-4C>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-4C>G
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
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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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  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 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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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: 594
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-73815819-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815819
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815819
    reference: chr 0
allele count: 1
allele frequency: 1.228999471530227e-5
allele num: 81367
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-7C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-7C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
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  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 depth: GenotypeDepth
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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
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4407
  num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

X-73815822-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815822
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815822
    reference: chr 0
allele count: 3
allele frequency: 3.696766561514196e-5
allele num: 81152
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-10G>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-10G>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
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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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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: 590
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-73815825-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815825
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815825
    reference: chr 0
allele count: 1
allele frequency: 1.239326302222112e-5
allele num: 80689
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-13C>T
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-13C>T
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.240645305848084e-5
  allele num: 44630
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
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site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
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site quality: DP
site quality: QD

X-73815835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815835
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815835
    reference: chr 0
allele count: 1
allele frequency: 1.269502735778396e-5
allele num: 78771
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-23G>A
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-23G>A
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.-23G>A
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8959
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

X-73815840-AAAGAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815840
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815835
    reference: chr 0
allele count: 40
allele frequency: 5.188942363822693e-4
allele num: 77087
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-23-10_-23-6delCTCTT
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-23-10_-23-6delCTCTT
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  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 quality: GenotypeQuality
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hgvs: c.-23-10_-23-6delCTCTT
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 25
  allele frequency: 5.832672297139658e-4
  allele num: 42862
  num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: AAAGAG
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

X-73815845-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815845
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815843
    reference: chr 0
allele count: 125
allele frequency: 1.626714557143229e-3
allele num: 76842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-23-12_-23-11delTT
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-23-12_-23-11delTT
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 8880
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: GAA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-73815850-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815850
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815850
    reference: chr 0
allele count: 1
allele frequency: 1.317905058119613e-5
allele num: 75878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-23-15C>G
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-23-15C>G
  variant of: http://identifiers.org/hgnc/13429
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  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 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 frequency: 1.605136436597111e-4
  allele num: 6230
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
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site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
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site quality: DP
site quality: ClippingRankSum

X-73815852-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073815852
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073815852
    reference: chr 0
allele count: 1
allele frequency: 1.339279735358324e-5
allele num: 74667
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000253571
  ensembl transcript: ENST00000349225
  gene symbol: RLIM
  hgvsc: ENST00000349225.2:c.-23-17C>A
  variant of: http://identifiers.org/hgnc/13429
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131263
  ensembl protein: ENSP00000328059
  ensembl transcript: ENST00000332687
  gene symbol: RLIM
  hgvsc: ENST00000332687.6:c.-23-17C>A
  variant of: http://identifiers.org/hgnc/13429
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: Latino
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  allele num: 8751
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population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
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X-73959200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959200
    reference: chr 0
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    type: ExactPosition
    position: 24073959200
    reference: chr 0
allele count: 1
allele frequency: 2.10300519442283e-5
allele num: 47551
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.*40T>C
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.*36+4T>C
  variant of: http://identifiers.org/hgnc/29433
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: South Asian
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  allele num: 5414
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population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
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site quality: MQ
site quality: VQSLOD
site quality: DP
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X-73959207-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959207
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959207
    reference: chr 0
allele count: 5
allele frequency: 1.036076172320189e-4
allele num: 48259
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.*33T>C
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.*33T>C
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Other
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population: European (Non-Finnish)
population: Latino
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population: South Asian
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site quality: BaseQRankSum
site quality: DP
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X-73959230-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959230
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959230
    reference: chr 0
allele count: 1
allele frequency: 1.811364500878512e-5
allele num: 55207
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.*10T>C
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.*10T>C
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.75e1
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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: 1338
  bin: 3.75e1
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6542
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

X-73959262-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959262
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959262
    reference: chr 0
allele count: 1
allele frequency: 1.446068861799199e-5
allele num: 69153
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.333G>A
  hgvsp: ENSP00000407055.1:p.Arg112His
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4529G>A
  hgvsp: ENSP00000055682.5:p.Arg1510His
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1
hgvs: p.Arg1510His
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7964
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

X-73959267-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959267
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959267
    reference: chr 0
allele count: 1
allele frequency: 1.409622080320266e-5
allele num: 70941
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4524G>C
  hgvsp: ENSP00000055682.5:p.Glu1508Asp
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.328G>C
  hgvsp: ENSP00000407055.1:p.Glu110Asp
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Glu1508Asp
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.305994514823038e-4
  allele num: 7657
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

X-73959280-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959280
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959280
    reference: chr 0
allele count: 1
allele frequency: 1.378359751895245e-5
allele num: 72550
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4511T>C
  hgvsp: ENSP00000055682.5:p.Val1504Ala
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.315T>C
  hgvsp: ENSP00000407055.1:p.Val106Ala
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val1504Ala
num of homozygotes: 0
population: South Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 7775
  num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ

X-73959282-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959282
    reference: chr 0
allele count: 70
allele frequency: 9.62344821897469e-4
allele num: 72739
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4509T>C
  hgvsp: ENST00000055682.6:c.4509T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.313T>C
  hgvsp: ENST00000424929.1:c.313T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
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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: p.Pro1503Pro
num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 2.590673575129534e-4
  allele num: 7720
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-73959285-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959285
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959285
    reference: chr 0
allele count: 1
allele frequency: 1.373550903796495e-5
allele num: 72804
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4506A>G
  hgvsp: ENST00000055682.6:c.4506A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.310A>G
  hgvsp: ENST00000424929.1:c.310A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 90
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  variant carriers: 0
hgvs: p.Leu1502Leu
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8268
  num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-73959293-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959293
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959293
    reference: chr 0
allele count: 1
allele frequency: 1.380967505834588e-5
allele num: 72413
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4498T>A
  hgvsp: ENSP00000055682.5:p.Trp1500Arg
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.302T>A
  hgvsp: ENSP00000407055.1:p.Trp102Arg
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13640
  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 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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  variant carriers: 0
hgvs: p.Trp1500Arg
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7774
  num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

X-73959297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959297
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959297
    reference: chr 0
allele count: 1
allele frequency: 1.39289345757943e-5
allele num: 71793
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.298C>T
  hgvsp: ENST00000424929.1:c.298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4494C>T
  hgvsp: ENST00000055682.6:c.4494C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  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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genotype quality: GenotypeQuality
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hgvs: p.Thr1498Thr
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7675
  num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

X-73959297-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959297
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959297
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 71793
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.298C>A
  hgvsp: ENST00000424929.1:c.298C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4494C>A
  hgvsp: ENST00000055682.6:c.4494C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 171
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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
  all individuals: 883
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  variant carriers: 0
hgvs: p.Thr1498Thr
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 38249
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

X-73959298-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959298
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959298
    reference: chr 0
allele count: 3
allele frequency: 4.176527913128219e-5
allele num: 71830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.297C>A
  hgvsp: ENSP00000407055.1:p.Thr100Asn
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4493C>A
  hgvsp: ENSP00000055682.5:p.Thr1498Asn
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Thr1498Asn
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8143
  num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

X-73959299-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959299
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959299
    reference: chr 0
allele count: 1
allele frequency: 1.401856057420024e-5
allele num: 71334
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4492A>G
  hgvsp: ENSP00000055682.5:p.Thr1498Ala
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.296A>G
  hgvsp: ENSP00000407055.1:p.Thr100Ala
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Thr1498Ala
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3657
  num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

X-73959300-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959300
    reference: chr 0
allele count: 1
allele frequency: 1.401090048057389e-5
allele num: 71373
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4491A>T
  hgvsp: ENST00000055682.6:c.4491A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.295A>T
  hgvsp: ENST00000424929.1:c.295A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Thr1497Thr
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8097
  num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-73959300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959300
    reference: chr 0
allele count: 1
allele frequency: 1.401090048057389e-5
allele num: 71373
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.295A>G
  hgvsp: ENST00000424929.1:c.295A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4491A>G
  hgvsp: ENST00000055682.6:c.4491A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Thr1497Thr
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5776
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

X-73959300-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959300
    reference: chr 0
allele count: 1
allele frequency: 1.401090048057389e-5
allele num: 71373
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4491A>C
  hgvsp: ENST00000055682.6:c.4491A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.295A>C
  hgvsp: ENST00000424929.1:c.295A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Thr1497Thr
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.307360439273108e-4
  allele num: 7649
  num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-73959313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959313
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959313
    reference: chr 0
allele count: 1
allele frequency: 1.456834008333091e-5
allele num: 68642
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4478T>C
  hgvsp: ENSP00000055682.5:p.Leu1493Pro
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.282T>C
  hgvsp: ENSP00000407055.1:p.Leu95Pro
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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  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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hgvs: p.Leu1493Pro
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5541
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
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X-73959324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959324
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959324
    reference: chr 0
allele count: 1
allele frequency: 1.517727051966974e-5
allele num: 65888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.271C>T
  hgvsp: ENST00000424929.1:c.271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4467C>T
  hgvsp: ENST00000055682.6:c.4467C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asp1489Asp
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.385809312638581e-4
  allele num: 7216
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

X-73959326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959326
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959326
    reference: chr 0
allele count: 2
allele frequency: 3.073613032119256e-5
allele num: 65070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.269G>A
  hgvsp: ENSP00000407055.1:p.Asp91Asn
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4465G>A
  hgvsp: ENSP00000055682.5:p.Asp1489Asn
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 173
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asp1489Asn
num of homozygotes: 0
population: East Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 5216
  num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

X-73959327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959327
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959327
    reference: chr 0
allele count: 6
allele frequency: 9.288644631937457e-5
allele num: 64595
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.268C>T
  hgvsp: ENST00000424929.1:c.268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4464C>T
  hgvsp: ENST00000055682.6:c.4464C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1749
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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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hgvs: p.Ser1488Ser
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 5
  allele frequency: 1.479071143321994e-4
  allele num: 33805
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: G
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site quality: VQSLOD
site quality: MQRankSum
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site quality: MQ
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X-73959327-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
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    reference: chr 0
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    type: ExactPosition
    position: 24073959327
    reference: chr 0
allele count: 2
allele frequency: 3.096214877312485e-5
allele num: 64595
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
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  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4464C>A
  hgvsp: ENST00000055682.6:c.4464C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
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  ensembl transcript: ENST00000424929
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  hgvsc: ENST00000424929.1:c.268C>A
  hgvsp: ENST00000424929.1:c.268C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser1488Ser
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population: South Asian
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  allele num: 7306
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population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
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site quality: InbreedingCoeff
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X-73959335-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959335
    reference: chr 0
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    type: ExactPosition
    position: 24073959335
    reference: chr 0
allele count: 1
allele frequency: 1.631747274982051e-5
allele num: 61284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.262-2A>G
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4458-2A>G
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: South Asian
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  allele num: 7097
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
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population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
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site quality: QD
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X-73959361-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959361
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959361
    reference: chr 0
allele count: 1
allele frequency: 1.889037912990914e-5
allele num: 52937
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4458-28T>G
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.262-28T>G
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Latino
population: European (Finnish)
population: African
population: South Asian
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population: Other
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site quality: FS
site quality: VQSLOD
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X-73959370-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959370
    reference: chr 0
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    type: ExactPosition
    position: 24073959370
    reference: chr 0
allele count: 1
allele frequency: 2.001561217749845e-5
allele num: 49961
alternate allele: T
annotation: Annotation
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  ensembl protein: ENSP00000055682
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  gene symbol: KIAA2022
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  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
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  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.262-37T>A
  variant of: http://identifiers.org/hgnc/29433
canonical: true
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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
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  allele num: 6422
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

X-73959380-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959380
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959380
    reference: chr 0
allele count: 2
allele frequency: 4.284490145672665e-5
allele num: 46680
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4458-47A>G
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.262-47A>G
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
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population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
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site quality: ClippingRankSum
site quality: ReadPosRankSum
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site quality: VQSLOD
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X-73959382-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959382
    reference: chr 0
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    type: ExactPosition
    position: 24073959382
    reference: chr 0
allele count: 1
allele frequency: 2.160807277598911e-5
allele num: 46279
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.262-49A>G
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4458-49A>G
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  allele num: 5604
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population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
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site quality: MQRankSum
site quality: DP
site quality: VQSLOD
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X-73959384-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959384
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959383
    reference: chr 0
allele count: 1
allele frequency: 2.187752958935877e-5
allele num: 45709
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.262-52delG
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4458-52delG
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
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genotype depth: GenotypeDepth
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population: East Asian
population: Latino
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site quality: ReadPosRankSum
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X-73959887-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959887
    reference: chr 0
  end: Position
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    reference: chr 0
allele count: 1
allele frequency: 1.252803147041505e-5
allele num: 79821
alternate allele: T
annotation: Annotation
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  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.261+47delT
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
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  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4457+47delT
  variant of: http://identifiers.org/hgnc/29433
canonical: true
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genotype depth: GenotypeDepth
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site quality: DP
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site quality: FS
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site quality: ReadPosRankSum
site quality: MQRankSum

X-73959897-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959897
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959897
    reference: chr 0
allele count: 1
allele frequency: 1.2465719272002e-5
allele num: 80220
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4457+38T>C
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.261+38T>C
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
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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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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 343
  bin: 8.75e1
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4308
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

X-73959943-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959943
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959943
    reference: chr 0
allele count: 1
allele frequency: 1.174784427057635e-5
allele num: 85122
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4449A>G
  hgvsp: ENST00000055682.6:c.4449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.253A>G
  hgvsp: ENST00000424929.1:c.253A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18325
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genotype depth: GenotypeDepth
  all individuals: 406
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 138
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  variant carriers: 0
hgvs: p.Glu1483Glu
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.179662616491683e-4
  allele num: 8477
  num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

X-73959946-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959946
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959946
    reference: chr 0
allele count: 4
allele frequency: 4.681538353502961e-5
allele num: 85442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.250T>G
  hgvsp: ENSP00000407055.1:p.Phe84Leu
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4446T>G
  hgvsp: ENSP00000055682.5:p.Phe1482Leu
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 418
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hgvs: p.Phe1482Leu
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4470
  num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

X-73959947-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959947
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959947
    reference: chr 0
allele count: 4
allele frequency: 4.67562828755114e-5
allele num: 85550
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4445T>C
  hgvsp: ENSP00000055682.5:p.Phe1482Ser
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.249T>C
  hgvsp: ENSP00000407055.1:p.Phe84Ser
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  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 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: 365
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hgvs: p.Phe1482Ser
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 47421
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

X-73959962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959962
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959962
    reference: chr 0
allele count: 1
allele frequency: 1.15060234032516e-5
allele num: 86911
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.234C>T
  hgvsp: ENSP00000407055.1:p.Ser79Phe
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4430C>T
  hgvsp: ENSP00000055682.5:p.Ser1477Phe
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6686
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44093
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3335
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser1477Phe
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4498
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-73959970-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24073959970
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24073959970
    reference: chr 0
allele count: 13
allele frequency: 1.490586373747334e-4
allele num: 87214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000407055
  ensembl transcript: ENST00000424929
  gene symbol: KIAA2022
  hgvsc: ENST00000424929.1:c.226G>A
  hgvsp: ENST00000424929.1:c.226G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000050030
  ensembl protein: ENSP00000055682
  ensembl transcript: ENST00000055682
  gene symbol: KIAA2022
  hgvsc: ENST00000055682.6:c.4422G>A
  hgvsp: ENST00000055682.6:c.4422G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19427
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys1474Lys
num of homozygotes: 0
reference allele: C

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9129
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.051104711051315e-4
allele num: 47569
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
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: 9301
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 1.941e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.102e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.78e-2

DP
type: SiteQuality
SIO_000300: 1.973364e6

VQSLOD
type: SiteQuality
SIO_000300: -1.403e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-1

QD
type: SiteQuality
SIO_000300: 1.631e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8437
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.119811760715649e-5
allele num: 47174
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

FS
type: SiteQuality
SIO_000300: 1.1175e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.424e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.923334e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.461e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9279
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6593
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.119227753406659e-5
allele num: 47187
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8437
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.923082e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 2.791e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8187
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9273
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.642e1

VQSLOD
type: SiteQuality
SIO_000300: -9.856e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.391e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.621e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.901847e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.776e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8155
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.801e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 5.758e1

DP
type: SiteQuality
SIO_000300: 1.897101e6

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8155
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.123412748970145e-5
allele num: 47094
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.758e1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.801e0

QD
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.897101e6

VQSLOD
type: SiteQuality
SIO_000300: -1.608e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8419
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.255953014278722e-5
allele num: 46993
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9263
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 3.674e0

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.872031e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

QD
type: SiteQuality
SIO_000300: 1.645e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7917
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4487
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6571
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8413
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 3.873e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.861239e6

QD
type: SiteQuality
SIO_000300: 1.154e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 325
allele frequency: 6.937329234972677e-3
allele num: 46848
num of homozygotes: 2

Latino
type: Population
allele count: 2
allele frequency: 2.161928440168631e-4
allele num: 9251
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 9.518143961927424e-4
allele num: 8405
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 1.141118295930011e-3
allele num: 7887
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.069e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.884e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.157e0

DP
type: SiteQuality
SIO_000300: 1.858482e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.044e0

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

QD
type: SiteQuality
SIO_000300: 1.834e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9251
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.134562841530055e-5
allele num: 46848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4485
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7887
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.044e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 1.157e0

QD
type: SiteQuality
SIO_000300: 1.834e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.884e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

DP
type: SiteQuality
SIO_000300: 1.858482e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.069e1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.139952921035737e-5
allele num: 46730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 593
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6539
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4480
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.248e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.089e-1

DP
type: SiteQuality
SIO_000300: 1.840406e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7641
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.148043132706105e-5
allele num: 46554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.839061e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.244e1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 489
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3955
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7671
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.737015806843842e-4
allele num: 5757
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37171
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.095323e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.924e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.751e1

VQSLOD
type: SiteQuality
SIO_000300: -2.86e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

FS
type: SiteQuality
SIO_000300: 6.315e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5813
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.32509718302359e-5
allele num: 37558
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.425418384671356e-4
allele num: 8246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
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MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.557e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 2.58e0

DP
type: SiteQuality
SIO_000300: 1.129836e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

QD
type: SiteQuality
SIO_000300: 1.449e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5885
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5459
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

FS
type: SiteQuality
SIO_000300: 5.902e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 1.202e1

DP
type: SiteQuality
SIO_000300: 1.162945e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.330000000000001e-1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.589935510605786e-5
allele num: 38611
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4033
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5580
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.066e0

DP
type: SiteQuality
SIO_000300: 1.190214e6

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -3.423e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.154e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

Latino
type: Population
allele count: 2
allele frequency: 2.356545304583481e-4
allele num: 8487
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 523
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 2.014e1

MQ
type: SiteQuality
SIO_000300: 6.037e1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 1.226855e6

VQSLOD
type: SiteQuality
SIO_000300: -2.327e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.77e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4155
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.960159362549801e-5
allele num: 40160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 523
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.036e-1

QD
type: SiteQuality
SIO_000300: 2.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 1.25238e6

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 2.987e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.753480773451025e-5
allele num: 41011
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4211
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 529
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.62e-2

DP
type: SiteQuality
SIO_000300: 1.284073e6

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

QD
type: SiteQuality
SIO_000300: 1.427e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 4.631e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.065e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4237
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41523
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6367
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

QD
type: SiteQuality
SIO_000300: 2.244e1

DP
type: SiteQuality
SIO_000300: 1.298193e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

Latino
type: Population
allele count: 1
allele frequency: 1.142595978062157e-4
allele num: 8752
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8135
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41681
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.427e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.447e0

DP
type: SiteQuality
SIO_000300: 1.303593e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.777e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8319
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.279981760145919e-4
allele num: 4386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.021e0

QD
type: SiteQuality
SIO_000300: 1.664e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.217e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
type: SiteQuality
SIO_000300: 1.395324e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8383
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9131
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4435
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.189860943830067e-5
allele num: 45665
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.576e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.957e1

MQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.450806e6

Latino
type: Population
allele count: 15
allele frequency: 1.634164941714784e-3
allele num: 9179
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.138607971445568e-4
allele num: 8405
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6527
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.478280340349306e-4
allele num: 4466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 140
allele frequency: 3.028467595396729e-3
allele num: 46228
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.476511e6

QD
type: SiteQuality
SIO_000300: 1.87e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.508e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.666e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6547
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8417
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9627
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9197
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 5.88e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.48509e6

VQSLOD
type: SiteQuality
SIO_000300: -1.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 2.376e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.130560763592978e-5
allele num: 46936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4489
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8445
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.503762e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.105e-1

QD
type: SiteQuality
SIO_000300: 3.046e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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African
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allele count: 414
allele frequency: 4.890148830616584e-2
allele num: 8466
num of homozygotes: 6

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.039e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.542992e6

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.211e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.092e0

QD
type: SiteQuality
SIO_000300: 1.686e1

South Asian
type: Population
allele count: 1
allele frequency: 1.035947373873407e-4
allele num: 9653
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6611
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.86e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.768e0

DP
type: SiteQuality
SIO_000300: 1.52483e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.57e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.302e0

MQ
type: SiteQuality
SIO_000300: 6.055e1

QD
type: SiteQuality
SIO_000300: 2.104e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.108770375993758e-5
allele num: 47421
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6613
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

DP
type: SiteQuality
SIO_000300: 1.526652e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
type: SiteQuality
SIO_000300: -1.712e0

QD
type: SiteQuality
SIO_000300: 1.15e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 1.2005e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9655
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4504
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47438
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
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East Asian
type: Population
allele count: 1
allele frequency: 1.512172992590352e-4
allele num: 6613
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.987e0

MQRankSum
type: SiteQuality
SIO_000300: -1.167e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.961e0

VQSLOD
type: SiteQuality
SIO_000300: -1.172e0

MQ
type: SiteQuality
SIO_000300: 5.596e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

DP
type: SiteQuality
SIO_000300: 1.527121e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.29e-1

QD
type: SiteQuality
SIO_000300: 1.506e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8457
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.060782857749019e-4
allele num: 9427
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

QD
type: SiteQuality
SIO_000300: 3.293e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.519145e6

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

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: 8409
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46981
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6591
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South Asian
type: Population
allele count: 1
allele frequency: 1.120197154699227e-4
allele num: 8927
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
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QD
type: SiteQuality
SIO_000300: 3.048e1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-2

DP
type: SiteQuality
SIO_000300: 1.490797e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.137009664582149e-4
allele num: 8795
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9225
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.479852e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.95e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

QD
type: SiteQuality
SIO_000300: 3.283e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46675
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084598698481562e-4
allele num: 9220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4490
num of homozygotes: 0

African
type: Population
allele count: 0
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allele num: 8368
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e0

VQSLOD
type: SiteQuality
SIO_000300: 2.39e-1

FS
type: SiteQuality
SIO_000300: 3.176e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.17e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.615e1

DP
type: SiteQuality
SIO_000300: 1.47118e6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8295
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4462
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VQSLOD
type: SiteQuality
SIO_000300: -2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.430513e6

QD
type: SiteQuality
SIO_000300: 3.133e1

South Asian
type: Population
allele count: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.406353962413801e-5
allele num: 45389
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4425
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
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DP
type: SiteQuality
SIO_000300: 1.379814e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.969e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

QD
type: SiteQuality
SIO_000300: 2.44e1

VQSLOD
type: SiteQuality
SIO_000300: -1.702e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6423
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 589
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8111
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44993
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.285016705217168e-4
allele num: 7782
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DP
type: SiteQuality
SIO_000300: 1.347874e6

MQ
type: SiteQuality
SIO_000300: 5.866e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -2.016e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.386e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4397
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7691
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African
type: Population
allele count: 0
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East Asian
type: Population
allele count: 3
allele frequency: 4.672169444011836e-4
allele num: 6421
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9057
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VQSLOD
type: SiteQuality
SIO_000300: -2.87e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.026e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.341666e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.14e-1

QD
type: SiteQuality
SIO_000300: 1.716e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4389
num of homozygotes: 0

Latino
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African
type: Population
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Other
type: Population
allele count: 0
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East Asian
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South Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 1.4405e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.316267e6

QD
type: SiteQuality
SIO_000300: 1.023e1

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 6285
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 575
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.287439668778736e-5
allele num: 43717
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.862e0

VQSLOD
type: SiteQuality
SIO_000300: -6.069e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.94e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

Other
type: Population
allele count: 0
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East Asian
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African
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allele frequency: 1.286670097786928e-4
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South Asian
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allele frequency: 2.15119852489244e-3
allele num: 6508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4309
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MQ
type: SiteQuality
SIO_000300: 5.022e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.87e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.637e0

FS
type: SiteQuality
SIO_000300: 3.847e0

DP
type: SiteQuality
SIO_000300: 1.168761e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

East Asian
type: Population
allele count: 18
allele frequency: 2.911208151382824e-3
allele num: 6183
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 4.407330085826954e-3
allele num: 4311
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 8.880994671403197e-3
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European (Non-Finnish)
type: Population
allele count: 52
allele frequency: 1.217285453438831e-3
allele num: 42718
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.292824822236587e-4
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num of homozygotes: 0

South Asian
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allele count: 30
allele frequency: 4.649721016738995e-3
allele num: 6452
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MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

QD
type: SiteQuality
SIO_000300: 2.552e1

MQ
type: SiteQuality
SIO_000300: 6.07e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.649e-1

DP
type: SiteQuality
SIO_000300: 1.158645e6

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4288
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 557
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.876e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.352e0

QD
type: SiteQuality
SIO_000300: 1.326e1

VQSLOD
type: SiteQuality
SIO_000300: -1.325e0

MQRankSum
type: SiteQuality
SIO_000300: -5.71e-1

DP
type: SiteQuality
SIO_000300: 1.12779e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.052e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7559
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.40639137549331e-5
allele num: 41556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5953
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6036
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.105413e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

QD
type: SiteQuality
SIO_000300: 1.247e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3549
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5465
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2563
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.1221814584278e-5
allele num: 24259
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 355
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.468e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.957e0

DP
type: SiteQuality
SIO_000300: 7.99558e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 3.4e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2601
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24618
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 8.991188635137566e-4
allele num: 5561
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5995
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.43e0

DP
type: SiteQuality
SIO_000300: 8.27845e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.336e0

QD
type: SiteQuality
SIO_000300: 1.431e1

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.335e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4371
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.53456807578114e-5
allele num: 28292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6465
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2907
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.512e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

QD
type: SiteQuality
SIO_000300: 1.415e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

DP
type: SiteQuality
SIO_000300: 9.93237e5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7487
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.78699070764832e-4
allele num: 5596
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 499
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 1.271e0

VQSLOD
type: SiteQuality
SIO_000300: -2.284e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 5.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

DP
type: SiteQuality
SIO_000300: 1.217344e6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8117
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5725
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7595
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37733
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

DP
type: SiteQuality
SIO_000300: 1.24108e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 4.42e0

VQSLOD
type: SiteQuality
SIO_000300: -2.194e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3729
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.583512026248482e-5
allele num: 38707
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5873
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: -1.717e0

DP
type: SiteQuality
SIO_000300: 1.26446e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 5.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

European (Non-Finnish)
type: Population
allele count: 67
allele frequency: 1.726181274797753e-3
allele num: 38814
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5897
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.678093197643278e-4
allele num: 3734
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.595e-1

QD
type: SiteQuality
SIO_000300: 1.59e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

DP
type: SiteQuality
SIO_000300: 1.269649e6

FS
type: SiteQuality
SIO_000300: 1.096e0

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7807
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.29366106080207e-4
allele num: 7730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5895
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38854
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

DP
type: SiteQuality
SIO_000300: 1.268854e6

FS
type: SiteQuality
SIO_000300: 3.963e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.133e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.51e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7715
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 517
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5841
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3715
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8201
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.58732212160414e-5
allele num: 38650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.259452e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.328e1

VQSLOD
type: SiteQuality
SIO_000300: -1.747e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

Latino
type: Population
allele count: 1
allele frequency: 1.228501228501228e-4
allele num: 8140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5803
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 509
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38249
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7737
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.48e0

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 8.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-2

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.244689e6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7737
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5803
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 509
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

DP
type: SiteQuality
SIO_000300: 1.244689e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

QD
type: SiteQuality
SIO_000300: 9.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 8.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3679
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5805
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.837604827964574e-5
allele num: 38277
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.394e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.041e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.302e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.095e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.1e-2

DP
type: SiteQuality
SIO_000300: 1.245113e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7641
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5771
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.235788433020267e-4
allele num: 8092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37957
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.234316e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: -1.434e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

FS
type: SiteQuality
SIO_000300: 3.0e0

QD
type: SiteQuality
SIO_000300: 5.82e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7649
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3660
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.296680497925311e-4
allele num: 7712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37973
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.372e0

MQRankSum
type: SiteQuality
SIO_000300: -1.782e0

DP
type: SiteQuality
SIO_000300: 1.234529e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

VQSLOD
type: SiteQuality
SIO_000300: -2.233e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

QD
type: SiteQuality
SIO_000300: 1.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.633450082953678e-5
allele num: 37973
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3660
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 8097
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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South Asian
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allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 506
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 37973
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 8097
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 5776
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3660
num of homozygotes: 0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.234529e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 36245
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African
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allele frequency: 1.346257404415724e-4
allele num: 7428
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7857
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7560
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 492
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.65e-1

Latino
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allele frequency: 0.0e0
allele num: 7578
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3396
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 34541
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South Asian
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allele count: 0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 467
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East Asian
type: Population
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.694e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

FS
type: SiteQuality
SIO_000300: 1.6699e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.113e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 467
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7478
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 7145
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European (Non-Finnish)
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allele count: 2
allele frequency: 5.872507854479255e-5
allele num: 34057
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3354
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FS
type: SiteQuality
SIO_000300: 8.163e0

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.72e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.315e0

QD
type: SiteQuality
SIO_000300: 2.685e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3338
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South Asian
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allele frequency: 1.368738023542294e-4
allele num: 7306
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 467
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7423
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 7104
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FS
type: SiteQuality
SIO_000300: 6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 8.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.062e0

DP
type: SiteQuality
SIO_000300: 1.09071e6

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.958142286643988e-5
allele num: 33805
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7423
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Other
type: Population
allele count: 0
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allele num: 467
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East Asian
type: Population
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allele frequency: 1.940993788819876e-4
allele num: 5152
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 7104
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3338
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

QD
type: SiteQuality
SIO_000300: 8.0e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6819
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6988
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3211
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Other
type: Population
allele count: 1
allele frequency: 2.212389380530973e-3
allele num: 452
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4813
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31904
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.381e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2780
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African
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South Asian
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allele count: 0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.708098487095817e-5
allele num: 26968
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Other
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allele num: 414
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FS
type: SiteQuality
SIO_000300: 3.245e0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

QD
type: SiteQuality
SIO_000300: 1.068e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

DP
type: SiteQuality
SIO_000300: 8.64465e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.31e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2643
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 396
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25235
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East Asian
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allele frequency: 2.712967986977754e-4
allele num: 3686
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VQSLOD
type: SiteQuality
SIO_000300: 1.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.96e-2

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

African
type: Population
allele count: 0
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allele num: 5656
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Other
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allele count: 0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6248
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2523
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 8.553588230262595e-5
allele num: 23382
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.27e-2

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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VQSLOD
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DP
type: SiteQuality
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QD
type: SiteQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 376
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele num: 2503
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South Asian
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East Asian
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allele num: 3331
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Latino
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allele frequency: 1.979022362952701e-4
allele num: 5053
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5561
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 4.36700292589196e-5
allele num: 22899
num of homozygotes: 0

East Asian
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allele num: 3270
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Latino
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allele count: 0
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Other
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allele num: 374
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South Asian
type: Population
allele count: 0
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allele num: 6189
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
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SIO_000300: 8.06713e5

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-2

MQ
type: SiteQuality
SIO_000300: 5.855e1

African
type: Population
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6278
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.22005150519492e-5
allele num: 45044
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 552
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
type: SiteQuality
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FS
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.0e-1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8341
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45238
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South Asian
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allele frequency: 1.566661444461852e-4
allele num: 6383
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Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
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East Asian
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
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SIO_000300: 5.883e1

QD
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.5e0

Other
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allele count: 0
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South Asian
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East Asian
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allele count: 0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 6.32e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.716e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

East Asian
type: Population
allele count: 4
allele frequency: 6.038647342995169e-4
allele num: 6624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8483
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47387
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.426e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

DP
type: SiteQuality
SIO_000300: 1.63639e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.69e-2

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.794e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 4.599287110497873e-4
allele num: 8697
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9243
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: -1.995e0

FS
type: SiteQuality
SIO_000300: 2.575e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.140000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.638345e6

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.374e0

QD
type: SiteQuality
SIO_000300: 2.419e1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
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: 1.035732780942517e-4
allele num: 9655
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.32e-2

DP
type: SiteQuality
SIO_000300: 1.667216e6

MQRankSum
type: SiteQuality
SIO_000300: -1.166e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.836e0

FS
type: SiteQuality
SIO_000300: 4.077e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

QD
type: SiteQuality
SIO_000300: 1.366e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1