X-67867798-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867798
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867798
    reference: chr 0
allele count: 3
allele frequency: 8.986340762041697e-5
allele num: 33384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+29C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+29C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+29C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+29C>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21212
  bin: 7.5e0
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 17289
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

X-67867799-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867799
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867799
    reference: chr 0
allele count: 11
allele frequency: 3.316449589966232e-4
allele num: 33168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+30C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+30C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+30C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+30C>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 118
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

X-67867799-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867799
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867799
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 33168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+30C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+30C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+30C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+30C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

X-67867804-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867804
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867803
    reference: chr 0
allele count: 107
allele frequency: 3.293118306044565e-3
allele num: 32492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+36delT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+36delT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+36delT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+36delT
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype 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
  all individuals: 320
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  variant carriers: 0
num of homozygotes: 3
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: CT
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-67867805-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867805
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867805
    reference: chr 0
allele count: 1
allele frequency: 3.106940905983968e-5
allele num: 32186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+36T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+36T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+36T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+36T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17664
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4332
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16253
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

X-67867806-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867806
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867805
    reference: chr 0
allele count: 1
allele frequency: 3.113228106223343e-5
allele num: 32121
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+38delA
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+38delA
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+38delA
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+38delA
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 21064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 1.25e1
  variant carriers: 0
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
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15758
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 357
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17670
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: CA
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

X-67867807-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867807
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867806
    reference: chr 0
allele count: 2
allele frequency: 6.362537379907107e-5
allele num: 31434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+44delG
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+44delG
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+44delG
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+44delG
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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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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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2617
  bin: 2.5e0
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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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genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4083
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: AG
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-67867808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867808
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867808
    reference: chr 0
allele count: 105
allele frequency: 3.324047106496138e-3
allele num: 31588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+39G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+39G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+39G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+39G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 1.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17769
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21154
  bin: 7.5e0
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
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  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4793
  bin: 1.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 549
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3744
  bin: 1.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14830
  bin: 2.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 3
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

X-67867808-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867808
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867808
    reference: chr 0
allele count: 5
allele frequency: 1.58287957452197e-4
allele num: 31588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+39G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+39G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+39G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+39G>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17769
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21154
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
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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: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3744
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14830
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 4793
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

X-67867809-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867809
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867809
    reference: chr 0
allele count: 1
allele frequency: 3.236560183836618e-5
allele num: 30897
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+40G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+40G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+40G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+40G>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21426
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 627
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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: 155
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 641
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

X-67867809-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067867809
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067867809
    reference: chr 0
allele count: 5
allele frequency: 1.618280091918309e-4
allele num: 30897
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.45+40G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.45+40G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-114+40G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl transcript: ENST00000488088
  gene symbol: STARD8
  hgvsc: ENST00000488088.1:n.262+40G>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21426
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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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
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

X-67885300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885300
    reference: chr 0
allele count: 1
allele frequency: 2.0478794208597e-5
allele num: 48831
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.46-41A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.46-41A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-113-41A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  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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  bin: 8.25e1
  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: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
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  variant carriers: 0
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
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  variant carriers: 0
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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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15867
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5296
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

X-67885317-ACTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885317
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885314
    reference: chr 0
allele count: 274
allele frequency: 5.414912748759906e-3
allele num: 50601
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.46-18_46-16delTCT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.46-18_46-16delTCT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-113-18_-113-16delTCT
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23289
  bin: 7.5e0
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 10340
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  variant carriers: 57
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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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
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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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: 10675
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 4
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: ACTT
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

X-67885326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885326
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885326
    reference: chr 0
allele count: 1
allele frequency: 1.917361710286645e-5
allele num: 52155
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.46-15C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-113-15C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.46-15C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ

X-67885343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885343
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885343
    reference: chr 0
allele count: 131
allele frequency: 2.332538015027955e-3
allele num: 56162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.48C>T
  hgvsp: ENST00000523864.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-111C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.48C>T
  hgvsp: ENST00000374599.3:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 116
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 8.25e1
  variant carriers: 2
hgvs: c.48C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

X-67885353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885353
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885353
    reference: chr 0
allele count: 2
allele frequency: 3.437371098583803e-5
allele num: 58184
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.58C>T
  hgvsp: ENST00000374599.3:c.58C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-101C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.58C>T
  hgvsp: ENST00000523864.1:c.58C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 667
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  variant carriers: 0
hgvs: p.Leu20Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

X-67885355-GCAGGTGAAGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885355
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885344
    reference: chr 0
allele count: 1
allele frequency: 1.710688381004516e-5
allele num: 58456
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.61_71delCAGGTGAAGAA
  hgvsp: ENSP00000363727.3:p.Gln21GlufsTer3
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.61_71delCAGGTGAAGAA
  hgvsp: ENSP00000428031.1:p.Gln21GlufsTer3
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
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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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 297
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln21GlufsTer3
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: GCAGGTGAAGAA
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

X-67885367-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885367
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885367
    reference: chr 0
allele count: 1
allele frequency: 1.678781875870868e-5
allele num: 59567
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.72G>T
  hgvsp: ENSP00000363727.3:p.Lys24Asn
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-87G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.72G>T
  hgvsp: ENSP00000428031.1:p.Lys24Asn
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: p.Lys24Asn
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

X-67885384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885384
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885384
    reference: chr 0
allele count: 664
allele frequency: 1.111278472326823e-2
allele num: 59751
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+10C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+10C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+10C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19879
  bin: 7.5e0
  variant carriers: 71
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 17
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

X-67885385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885385
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885385
    reference: chr 0
allele count: 1
allele frequency: 1.67664269067619e-5
allele num: 59643
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+11G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+11G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+11G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

X-67885392-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885392
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885392
    reference: chr 0
allele count: 2
allele frequency: 3.366890003703579e-5
allele num: 59402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+18G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+18G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+18G>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

X-67885405-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885405
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885405
    reference: chr 0
allele count: 1
allele frequency: 1.697879348693482e-5
allele num: 58897
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+31C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+31C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+31C>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum

X-67885407-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885407
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885407
    reference: chr 0
allele count: 1
allele frequency: 1.69715895590781e-5
allele num: 58922
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+33T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+33T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+33T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

X-67885416-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885416
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885416
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 57899
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+42A>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+42A>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+42A>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
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 quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

X-67885418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067885418
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067885418
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 57606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.79+44T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-80+44T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.79+44T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 1
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

X-67932708-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932708
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932708
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 30678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.80-48C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-79-48C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
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  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.80-48C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
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  ensembl protein: ENSP00000363725
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  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-161-48C>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

X-67932708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932708
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932708
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 30678
alternate allele: T
annotation: Annotation
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  consequence: intron_variant
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  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.80-48C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
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  ensembl gene: ENSG00000130052
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  hgvsc: ENST00000523864.1:c.80-48C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
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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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num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
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population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
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site quality: QD
site quality: InbreedingCoeff
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site quality: DP

X-67932715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932715
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932715
    reference: chr 0
allele count: 1
allele frequency: 3.227576412871575e-5
allele num: 30983
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
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  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.80-41C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-79-41C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
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  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-161-41C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
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  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.80-41C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
population: East Asian
population: South Asian
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population: Other
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population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
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site quality: VQSLOD

X-67932718-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932718
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932718
    reference: chr 0
allele count: 1
allele frequency: 3.191625175539385e-5
allele num: 31332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
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  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.80-38C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
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  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

X-67932718-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932718
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932718
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 31332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-161-38C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.80-38C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.80-38C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-79-38C>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

X-67932738-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932738
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932738
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 34601
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.80-18T>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-161-18T>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-79-18T>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.80-18T>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.75e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  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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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 262
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

X-67932760-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932760
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932760
    reference: chr 0
allele count: 1
allele frequency: 2.323798015476495e-5
allele num: 43033
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.84C>T
  hgvsp: ENST00000523864.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-75C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.84C>T
  hgvsp: ENST00000374599.3:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-157C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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
  all individuals: 254
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  variant carriers: 0
hgvs: p.Ala28Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

X-67932761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932761
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932761
    reference: chr 0
allele count: 6
allele frequency: 1.372087173271742e-4
allele num: 43729
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.85G>A
  hgvsp: ENSP00000428031.1:p.Glu29Lys
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-74G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.85G>A
  hgvsp: ENSP00000363727.3:p.Glu29Lys
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-156G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 14547
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu29Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

X-67932771-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932771
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932771
    reference: chr 0
allele count: 1
allele frequency: 2.105972538118103e-5
allele num: 47484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-146G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.95G>T
  hgvsp: ENSP00000363727.3:p.Arg32Ile
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.95G>T
  hgvsp: ENSP00000428031.1:p.Arg32Ile
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-64G>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 265
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg32Ile
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

X-67932775-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932775
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932775
    reference: chr 0
allele count: 18
allele frequency: 3.712641544458883e-4
allele num: 48483
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-60A>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.99A>C
  hgvsp: ENST00000374599.3:c.99A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-142A>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.99A>C
  hgvsp: ENST00000523864.1:c.99A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 270
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hgvs: p.Ala33Ala
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

X-67932779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932779
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932779
    reference: chr 0
allele count: 12
allele frequency: 2.444041630175767e-4
allele num: 49099
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-56G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-138G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.103G>A
  hgvsp: ENSP00000428031.1:p.Glu35Lys
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.103G>A
  hgvsp: ENSP00000363727.3:p.Glu35Lys
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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.Glu35Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

X-67932797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932797
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932797
    reference: chr 0
allele count: 1
allele frequency: 1.966181675186787e-5
allele num: 50860
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.121G>A
  hgvsp: ENSP00000363727.3:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-120G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-38G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.121G>A
  hgvsp: ENSP00000428031.1:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.25e1
  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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  variant carriers: 0
hgvs: p.Gly41Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

X-67932813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932813
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932813
    reference: chr 0
allele count: 1
allele frequency: 2.024455421491619e-5
allele num: 49396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.137T>C
  hgvsp: ENSP00000363727.3:p.Val46Ala
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-22T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.137T>C
  hgvsp: ENSP00000428031.1:p.Val46Ala
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-104T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3899
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Val46Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

X-67932823-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932823
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932823
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 48387
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-94T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.147T>C
  hgvsp: ENST00000523864.1:c.147T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.147T>C
  hgvsp: ENST00000374599.3:c.147T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-12T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
hgvs: p.Phe49Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-67932833-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932833
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932833
    reference: chr 0
allele count: 1
allele frequency: 2.151416707902153e-5
allele num: 46481
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.151+6G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.151+6G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-8+6G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-90+6G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
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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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  variant carriers: 0
hgvs: c.151+6G>A
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-67932834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932834
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932834
    reference: chr 0
allele count: 4
allele frequency: 8.649396704579856e-5
allele num: 46246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-90+7C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.151+7C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.151+7C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-8+7C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22662
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 178
  bin: 4.75e1
  variant carriers: 0
hgvs: c.151+7C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

X-67932836-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932836
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932836
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 45909
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-90+9A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.151+9A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-8+9A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.151+9A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff

X-67932853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932853
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932853
    reference: chr 0
allele count: 1
allele frequency: 2.429779376032656e-5
allele num: 41156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-90+26C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.151+26C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-8+26C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.151+26C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
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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  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

X-67932870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932870
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932870
    reference: chr 0
allele count: 1
allele frequency: 2.830375590840904e-5
allele num: 35331
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-8+43C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.151+43C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.151+43C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-90+43C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
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site quality: ReadPosRankSum

X-67932875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067932875
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067932875
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 34136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-90+48G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.151+48G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-8+48G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.151+48G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

X-67935102-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935102
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935102
    reference: chr 0
allele count: 3
allele frequency: 8.238137082601055e-5
allele num: 36416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1108A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1108A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
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  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.152-34A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-89-34A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-67935118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935118
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935118
    reference: chr 0
allele count: 2
allele frequency: 5.026767537135245e-5
allele num: 39787
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1092C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-89-18C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1092C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.152-18C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
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site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-67935125-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935125
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935125
    reference: chr 0
allele count: 1
allele frequency: 2.361052084808991e-5
allele num: 42354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1085C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.152-11C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-89-11C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1085C>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
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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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num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

X-67935131-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935131
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935131
    reference: chr 0
allele count: 1
allele frequency: 2.201382468190023e-5
allele num: 45426
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-89-5T>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.152-5T>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1079T>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1079T>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2251
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.152-5T>G
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-67935140-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935140
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935140
    reference: chr 0
allele count: 3
allele frequency: 6.130080304051984e-5
allele num: 48939
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.156T>C
  hgvsp: ENST00000374599.3:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1070T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1070T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-85T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
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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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  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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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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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
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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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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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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: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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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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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly52Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

X-67935142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935142
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935142
    reference: chr 0
allele count: 2
allele frequency: 4.047354042294849e-5
allele num: 49415
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1068C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-83C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1068C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.158C>T
  hgvsp: ENSP00000363727.3:p.Ser53Leu
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16879
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
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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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  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser53Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

X-67935143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935143
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935143
    reference: chr 0
allele count: 314
allele frequency: 6.265339106490812e-3
allele num: 50117
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1067G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-82G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1067G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.159G>A
  hgvsp: ENST00000374599.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 1.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
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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: 29
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 52
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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  variant carriers: 18
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 199
  bin: 9.25e1
  variant carriers: 4
hgvs: p.Ser53Ser
num of homozygotes: 4
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-67935169-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935169
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935169
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 55594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1041A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.185A>G
  hgvsp: ENSP00000363727.3:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-56A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1041A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 578
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  variant carriers: 0
hgvs: p.Lys62Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-67935175-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935175
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935175
    reference: chr 0
allele count: 1
allele frequency: 1.798852332212049e-5
allele num: 55591
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-50A>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.191A>T
  hgvsp: ENSP00000363727.3:p.Asn64Ile
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1035A>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1035A>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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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  bin: 4.75e1
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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: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25280
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn64Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

X-67935180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935180
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935180
    reference: chr 0
allele count: 18
allele frequency: 3.254207871567263e-4
allele num: 55313
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-45G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1030G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1030G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.196G>A
  hgvsp: ENSP00000363727.3:p.Gly66Ser
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
genotype quality: GenotypeQuality
  all individuals: 349
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  variant carriers: 2
hgvs: p.Gly66Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-67935191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935191
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935191
    reference: chr 0
allele count: 10
allele frequency: 1.830663615560641e-4
allele num: 54625
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1019C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.207C>T
  hgvsp: ENST00000374599.3:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-34C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1019C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3227
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Asp69Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

X-67935192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935192
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935192
    reference: chr 0
allele count: 1
allele frequency: 1.833987455525804e-5
allele num: 54526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-33G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1018G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.208G>A
  hgvsp: ENSP00000363727.3:p.Glu70Lys
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1018G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
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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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  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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  bin: 5.75e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3407
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu70Lys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

X-67935202-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935202
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935202
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 53413
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-23T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.218T>C
  hgvsp: ENSP00000363727.3:p.Leu73Ser
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1008T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1008T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu73Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-67935204-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935204
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935204
    reference: chr 0
allele count: 1
allele frequency: 1.879840589518009e-5
allele num: 53196
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.220G>A
  hgvsp: ENSP00000363727.3:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1006G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1006G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-21G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1138
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  variant carriers: 0
hgvs: p.Gly74Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

X-67935207-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935207
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935207
    reference: chr 0
allele count: 1
allele frequency: 1.897821301146284e-5
allele num: 52692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-1003G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-1003G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-18G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.223G>C
  hgvsp: ENSP00000363727.3:p.Ala75Pro
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9813
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 903
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  variant carriers: 0
hgvs: p.Ala75Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

X-67935215-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935215
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935215
    reference: chr 0
allele count: 1
allele frequency: 1.938285005427198e-5
allele num: 51592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-995T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-10T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-995T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.231T>C
  hgvsp: ENST00000374599.3:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
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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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  variant carriers: 0
hgvs: c.231T>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

X-67935217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935217
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935217
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 51273
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233G>A
  hgvsp: ENSP00000363727.3:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-993G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-993G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: missense
filter: AC_Adj0_Filter
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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 7.25e1
  variant carriers: 0
hgvs: p.Arg78Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

X-67935220-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935220
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935220
    reference: chr 0
allele count: 1
allele frequency: 1.98625511460692e-5
allele num: 50346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-990A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+3A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+3A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-990A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 548
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  variant carriers: 0
hgvs: c.233+3A>G
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

X-67935226-GCTGAGGGCCAGGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935226
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935213
    reference: chr 0
allele count: 10
allele frequency: 2.023758929836278e-4
allele num: 49413
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: GCTGAGGGCCAGGC
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

X-67935236-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935236
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935236
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 47059
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-974A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-974A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+19A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+19A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14599
  bin: 1.25e1
  variant carriers: 1
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 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: 3404
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-67935240-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935240
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935240
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 46366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-970C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-970C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+23C>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+23C>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-67935241-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935241
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935241
    reference: chr 0
allele count: 4
allele frequency: 8.70738821890374e-5
allele num: 45938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-969T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-969T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+24T>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+24T>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

X-67935245-A-AACCAGTCACTCTAGCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935245
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935261
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 45369
alternate allele: AACCAGTCACTCTAGCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 21605
  bin: 7.5e0
  variant carriers: 1
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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS

X-67935251-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935251
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935251
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 43988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-959A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+34A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+34A>G
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-959A>G
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 397
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP

X-67935254-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935254
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935254
    reference: chr 0
allele count: 1
allele frequency: 2.325851843237586e-5
allele num: 42995
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-956G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-956G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+37G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+37G>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

X-67935258-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935258
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935258
    reference: chr 0
allele count: 1
allele frequency: 2.40610187435336e-5
allele num: 41561
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-952G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-952G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+41G>C
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+41G>C
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

X-67935260-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067935260
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067935260
    reference: chr 0
allele count: 26
allele frequency: 6.439309507888154e-4
allele num: 40377
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.233+43C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-950C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-8+43C>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-950C>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

X-67936169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067936169
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067936169
    reference: chr 0
allele count: 1
allele frequency: 1.535414331557371e-5
allele num: 65129
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.234-41G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-41G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-41G>A
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-7-41G>A
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16206
  bin: 1.25e1
  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 quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

X-67936184-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067936184
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067936184
    reference: chr 0
allele count: 1
allele frequency: 1.422940649145524e-5
allele num: 70277
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-26G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.234-26G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-7-26G>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-26G>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15129
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3833
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3980
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

X-67936193-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067936193
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067936192
    reference: chr 0
allele count: 3
allele frequency: 4.049293398301996e-5
allele num: 74087
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-15delT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-15delT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.234-15delT
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-7-15delT
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12451
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3667
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12970
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2348
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28879
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: CT
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

X-67936207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24067936207
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24067936207
    reference: chr 0
allele count: 1
allele frequency: 1.275949625508785e-5
allele num: 78373
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363725
  ensembl transcript: ENST00000374597
  gene symbol: STARD8
  hgvsc: ENST00000374597.3:c.-7-3C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000428031
  ensembl transcript: ENST00000523864
  gene symbol: STARD8
  hgvsc: ENST00000523864.1:c.152-3C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000252336
  ensembl transcript: ENST00000252336
  gene symbol: STARD8
  hgvsc: ENST00000252336.6:c.-7-3C>T
  variant of: http://identifiers.org/hgnc/19161
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130052
  ensembl protein: ENSP00000363727
  ensembl transcript: ENST00000374599
  gene symbol: STARD8
  hgvsc: ENST00000374599.3:c.234-3C>T
  variant of: http://identifiers.org/hgnc/19161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33404
  bin: 2.25e1
  variant carriers: 0
hgvs: c.234-3C>T
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.775722106852935e-4
allele num: 5297
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.998500749625187e-4
allele num: 3335
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2635
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18173
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

FS
type: SiteQuality
SIO_000300: 3.835e0

VQSLOD
type: SiteQuality
SIO_000300: -4.354e-1

DP
type: SiteQuality
SIO_000300: 6.66994e5

QD
type: SiteQuality
SIO_000300: 1.655e1

GenotypeQuality
all individuals: 1200
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 9.75e1
variant carriers: 7

South Asian
type: Population
allele count: 10
allele frequency: 1.896094046264695e-3
allele num: 5274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18045
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1527
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3330
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.831417624521073e-4
allele num: 2610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.35e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

FS
type: SiteQuality
SIO_000300: 1.1805e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.226e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 6.63668e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.703e1

GenotypeQuality
all individuals: 2254
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1527
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18045
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

FS
type: SiteQuality
SIO_000300: 1.1805e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 2.703e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.35e-2

DP
type: SiteQuality
SIO_000300: 6.63668e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.226e0

GenotypeQuality
all individuals: 4178
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 412
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2138
bin: 2.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3262
num of homozygotes: 0

East Asian
type: Population
allele count: 91
allele frequency: 4.224698235840297e-2
allele num: 2154
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.672793283412752e-5
allele num: 17628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2472
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 2.868068833652008e-3
allele num: 5230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.098e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

QD
type: SiteQuality
SIO_000300: 2.501e1

DP
type: SiteQuality
SIO_000300: 6.4625e5

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2473
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2435
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1500
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.042864346949068e-4
allele num: 1983
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.31e0

VQSLOD
type: SiteQuality
SIO_000300: -5.684e0

MQRankSum
type: SiteQuality
SIO_000300: 2.38e0

DP
type: SiteQuality
SIO_000300: 6.40642e5

QD
type: SiteQuality
SIO_000300: 4.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.383e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 249
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2393
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5205
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.743825387708214e-5
allele num: 17410
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.53e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.589e0

VQSLOD
type: SiteQuality
SIO_000300: -1.438e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 3.31e0

DP
type: SiteQuality
SIO_000300: 6.4081e5

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.123048094940662e-4
allele num: 3202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17009
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.945525291828794e-4
allele num: 5140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 243
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2079
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2289
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.654e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

DP
type: SiteQuality
SIO_000300: 6.36754e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.78e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.629999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.839e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2529
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2579
bin: 9.75e1
variant carriers: 120

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

East Asian
type: Population
allele count: 89
allele frequency: 4.278846153846154e-2
allele num: 2080
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.841462702260646e-5
allele num: 17119
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 245
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 2.918287937743191e-3
allele num: 5140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1483
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2321
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

DP
type: SiteQuality
SIO_000300: 6.36473e5

MQ
type: SiteQuality
SIO_000300: 6.066e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 2.424e1

GenotypeQuality
all individuals: 2579
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 2.920731351130323e-4
allele num: 17119
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2321
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1483
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 245
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.424e1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.36473e5

MQ
type: SiteQuality
SIO_000300: 6.066e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2467
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.958096729978461e-4
allele num: 5107
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1975
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2207
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16761
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3165
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.596e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 6.31144e5

GenotypeQuality
all individuals: 13077
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3165
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.966231131794045e-5
allele num: 16761
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2207
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 2.025316455696203e-3
allele num: 1975
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5107
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.596e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.67e-1

DP
type: SiteQuality
SIO_000300: 6.31144e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.39e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

GenotypeQuality
all individuals: 1395
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.894687646050787e-5
allele num: 25676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6221
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2543
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4867
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.41e0

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

DP
type: SiteQuality
SIO_000300: 1.163886e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

FS
type: SiteQuality
SIO_000300: 3.282e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.44e-2

GenotypeQuality
all individuals: 275
bin: 5.25e1
variant carriers: 4

Latino
type: Population
allele count: 7
allele frequency: 1.374165685119749e-3
allele num: 5094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.502460278706382e-4
allele num: 26623
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2617
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.666666666666667e-3
allele num: 375
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4079
num of homozygotes: 0

African
type: Population
allele count: 262
allele frequency: 4.777534646243618e-2
allele num: 5484
num of homozygotes: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6329
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

MQ
type: SiteQuality
SIO_000300: 5.701e1

DP
type: SiteQuality
SIO_000300: 1.245346e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

MQRankSum
type: SiteQuality
SIO_000300: -5.27e-1

FS
type: SiteQuality
SIO_000300: 1.176e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.98e-2

QD
type: SiteQuality
SIO_000300: 2.084e1

GenotypeQuality
all individuals: 2577
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5323
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4231
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2677
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.626867836936022e-5
allele num: 27572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-3

FS
type: SiteQuality
SIO_000300: 1.1896e1

DP
type: SiteQuality
SIO_000300: 1.288423e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.581e0

VQSLOD
type: SiteQuality
SIO_000300: -1.188e0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

QD
type: SiteQuality
SIO_000300: 2.198e1

MQ
type: SiteQuality
SIO_000300: 5.988e1

GenotypeQuality
all individuals: 645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6591
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29819
num of homozygotes: 0

African
type: Population
allele count: 125
allele frequency: 2.116850127011008e-2
allele num: 5905
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4627
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 1.005867560771165e-3
allele num: 5965
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2847
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.758e0

DP
type: SiteQuality
SIO_000300: 1.356326e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.614e1

VQSLOD
type: SiteQuality
SIO_000300: 5.67e0

GenotypeQuality
all individuals: 341
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31078
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.202049311559398e-4
allele num: 6246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.045e0

QD
type: SiteQuality
SIO_000300: 1.399e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.449e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

DP
type: SiteQuality
SIO_000300: 1.382955e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 585
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31245
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6283
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.65508109897385e-4
allele num: 6042
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.335e0

FS
type: SiteQuality
SIO_000300: 1.2509e1

MQRankSum
type: SiteQuality
SIO_000300: -1.009e1

QD
type: SiteQuality
SIO_000300: 3.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 1.38666e6

VQSLOD
type: SiteQuality
SIO_000300: -4.328e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

MQ
type: SiteQuality
SIO_000300: 5.186e1

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4917
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6133
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.139323161926289e-5
allele num: 31854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2991
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.589e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.392298e6

QD
type: SiteQuality
SIO_000300: 6.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

GenotypeQuality
all individuals: 332
bin: 4.25e1
variant carriers: 7

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2983
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.320185614849188e-3
allele num: 431
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6783
num of homozygotes: 0

Latino
type: Population
allele count: 33
allele frequency: 5.083962409490063e-3
allele num: 6491
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4884
num of homozygotes: 0

African
type: Population
allele count: 615
allele frequency: 9.862091084028224e-2
allele num: 6236
num of homozygotes: 16

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 4.695864508656044e-4
allele num: 31943
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.365812e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.888e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.673e1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6173
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 429
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.135779241141423e-5
allele num: 31890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2983
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.182e0

FS
type: SiteQuality
SIO_000300: 1.115e0

QD
type: SiteQuality
SIO_000300: 5.13e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-1

DP
type: SiteQuality
SIO_000300: 1.353994e6

VQSLOD
type: SiteQuality
SIO_000300: -2.141e0

GenotypeQuality
all individuals: 5293
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4864
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South Asian
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allele frequency: 1.479071143321994e-4
allele num: 6761
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 3.146633102580239e-5
allele num: 31780
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2965
num of homozygotes: 0

FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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MQ
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QD
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2939
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 6367
num of homozygotes: 0

African
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allele frequency: 1.649348507339601e-4
allele num: 6063
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 31565
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2938
num of homozygotes: 0

African
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allele frequency: 1.650437365901964e-4
allele num: 6059
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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DP
type: SiteQuality
SIO_000300: 1.285362e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31018
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2881
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6653
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2874
num of homozygotes: 0

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

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

FS
type: SiteQuality
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VQSLOD
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QD
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DP
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InbreedingCoeff
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SIO_000300: -1.25e-2

MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1895
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3629
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

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

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

MQRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.97e-2

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.26706e5

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2024
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3629
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2204
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1895
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.26706e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 3653
num of homozygotes: 0

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 251
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1912
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.195403010965863e-5
allele num: 16141
num of homozygotes: 0

QD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.43756e5

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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VQSLOD
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
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allele frequency: 0.0e0
allele num: 3691
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1928
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 6.142506142506142e-5
allele num: 16280
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2276
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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MQ
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1928
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2276
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 253
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East Asian
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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DP
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MQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 17876
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 2.979737783075089e-4
allele num: 3356
num of homozygotes: 0

African
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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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Other
type: Population
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allele frequency: 0.0e0
allele num: 325
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 5808
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2407
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.328315253486827e-4
allele num: 22585
num of homozygotes: 0

Latino
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allele frequency: 4.630701551285019e-4
allele num: 4319
num of homozygotes: 0

African
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2443
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 1.710571330824495e-4
allele num: 5846
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Other
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MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele num: 5099
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4844
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.121794e6

FS
type: SiteQuality
SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.536e0

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.054e0

QD
type: SiteQuality
SIO_000300: 4.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.08e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6105
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2626
num of homozygotes: 0

East Asian
type: Population
allele count: 18
allele frequency: 4.595353586928772e-3
allele num: 3917
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4987
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25324
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.653e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.131769e6

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.653e-1

FS
type: SiteQuality
SIO_000300: 5.137e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.04e-2

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3979
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 3.118786791937936e-4
allele num: 25651
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 369
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 1.509433962264151e-3
allele num: 2650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5193
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5113
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.57e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.554e0

DP
type: SiteQuality
SIO_000300: 1.13907e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

FS
type: SiteQuality
SIO_000300: 1.762e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2695
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4149
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5354
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.596933886937081e-4
allele num: 6262
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.186e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e0

FS
type: SiteQuality
SIO_000300: 1.332e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.741000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 1.150962e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6195
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5251
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.853861569292431e-5
allele num: 25948
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 369
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.823e-1

DP
type: SiteQuality
SIO_000300: 1.108275e6

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

FS
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

QD
type: SiteQuality
SIO_000300: 1.233e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.61e-1

MQ
type: SiteQuality
SIO_000300: 5.878e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
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GenotypeQuality
all individuals: 168
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GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5167
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25423
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6155
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3857
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 357
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.075785e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.699e-1

QD
type: SiteQuality
SIO_000300: 2.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3900
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variant carriers: 1

GenotypeQuality
all individuals: 1016
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.008435428800964e-4
allele num: 4979
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4545
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24419
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3681
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 349
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.186e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

FS
type: SiteQuality
SIO_000300: 1.632e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

DP
type: SiteQuality
SIO_000300: 1.023836e6

QD
type: SiteQuality
SIO_000300: 1.287e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 5.010856856522465e-4
allele num: 5987
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2485
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.018163471241171e-4
allele num: 4955
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24290
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

FS
type: SiteQuality
SIO_000300: 2.897e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

DP
type: SiteQuality
SIO_000300: 1.017821e6

VQSLOD
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5961
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4441
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 343
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24118
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.87e-2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3695
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5595
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.83e-2

DP
type: SiteQuality
SIO_000300: 9.14444e5

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 281
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4005
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 1.940993788819876e-4
allele num: 5152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2795
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 18423
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.45e-2

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 281
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 17719
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3987
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2201
num of homozygotes: 0

South Asian
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allele frequency: 4.730368968779565e-4
allele num: 4228
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 5.027652086475616e-5
allele num: 19890
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 275
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VQSLOD
type: SiteQuality
SIO_000300: 6.44e-1

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

GenotypeQuality
all individuals: 3418
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 763
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4621
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3646
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.323420074349442e-4
allele num: 4304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2961
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.629843974258068e-5
allele num: 21599
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.54e0

DP
type: SiteQuality
SIO_000300: 9.28358e5

QD
type: SiteQuality
SIO_000300: 2.577e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

MQRankSum
type: SiteQuality
SIO_000300: -1.19e0

FS
type: SiteQuality
SIO_000300: 3.496e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.59e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.471e0

GenotypeQuality
all individuals: 1304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 321
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.466091245376079e-4
allele num: 4055
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4895
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

FS
type: SiteQuality
SIO_000300: 1.683e0

QD
type: SiteQuality
SIO_000300: 1.797e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.837e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 9.75251e5

GenotypeQuality
all individuals: 329
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 337
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3499
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2543
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4489
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4735
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.071163945772096e-5
allele num: 24563
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5260
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.766e1

VQSLOD
type: SiteQuality
SIO_000300: -3.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.15e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.588e1

DP
type: SiteQuality
SIO_000300: 1.019975e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.818e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5071
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2629
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.135718341851221e-4
allele num: 26415
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5021
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3823
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

DP
type: SiteQuality
SIO_000300: 1.068155e6

FS
type: SiteQuality
SIO_000300: 2.433e0

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

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

GenotypeQuality
all individuals: 279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 3.951007506914263e-4
allele num: 5062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2651
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26670
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.48e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

DP
type: SiteQuality
SIO_000300: 1.077026e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.623e0

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

GenotypeQuality
all individuals: 17738
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 272
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1146
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 3
allele frequency: 8.264462809917356e-3
allele num: 363
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.757985719654265e-4
allele num: 2661
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.480682213713888e-4
allele num: 5746
num of homozygotes: 0

African
type: Population
allele count: 146
allele frequency: 2.829457364341085e-2
allele num: 5160
num of homozygotes: 3

Latino
type: Population
allele count: 66
allele frequency: 1.255946717411989e-2
allele num: 5255
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3941
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 96
allele frequency: 3.5567411359342e-3
allele num: 26991
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.087566e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.631e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 1.657e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeQuality
all individuals: 25240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2869
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6249
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5557
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29969
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6071
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 403
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.137e0

DP
type: SiteQuality
SIO_000300: 1.144088e6

QD
type: SiteQuality
SIO_000300: 2.089e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.519e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

GenotypeQuality
all individuals: 512
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2873
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.334444814938313e-5
allele num: 29990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 407
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6243
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5558
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e-1

QD
type: SiteQuality
SIO_000300: 1.528e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

DP
type: SiteQuality
SIO_000300: 1.138592e6

GenotypeQuality
all individuals: 417
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2869
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.351543385729128e-5
allele num: 29837
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4447
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.99700449326011e-3
allele num: 6009
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 8.063215610385422e-4
allele num: 6201
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.132037e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

FS
type: SiteQuality
SIO_000300: 1.795e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5921
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.387419125368382e-5
allele num: 29521
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 401
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4384
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 1.483434976100214e-3
allele num: 6067
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5491
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.572000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.109126e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 7.991e0

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.887e1

GenotypeQuality
all individuals: 1411
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.25e1
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GenotypeQuality
all individuals: 1206
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 399
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5927
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4367
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2839
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.39328130302002e-5
allele num: 29470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.104819e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.81e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.45e-1

QD
type: SiteQuality
SIO_000300: 2.81e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.927e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2819
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28927
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5417
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5751
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4302
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.654e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 1.073302e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
all individuals: 710
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variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2801
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5397
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.468007629616785e-5
allele num: 28835
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5727
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.323e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

FS
type: SiteQuality
SIO_000300: 1.312e0

DP
type: SiteQuality
SIO_000300: 1.066548e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.107e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 5.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5359
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5657
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2800
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.763357432551578e-4
allele num: 5671
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 383
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.053341e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 4.899e0

VQSLOD
type: SiteQuality
SIO_000300: -2.927e0

QD
type: SiteQuality
SIO_000300: 2.118e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

GenotypeQuality
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 278
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2761
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.562268452550584e-5
allele num: 28072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5259
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4148
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

DP
type: SiteQuality
SIO_000300: 1.016164e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

FS
type: SiteQuality
SIO_000300: 5.167e0

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 6.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 274
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4109
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27901
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5453
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.713e0

DP
type: SiteQuality
SIO_000300: 1.007236e6

VQSLOD
type: SiteQuality
SIO_000300: -9.165e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.871e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 1122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.877229209686503e-4
allele num: 5327
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4027
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.141e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.554e0

DP
type: SiteQuality
SIO_000300: 9.8082e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 7.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26936
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 1.92789666473877e-3
allele num: 5187
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2689
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3919
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 371
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5199
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.38e-1

FS
type: SiteQuality
SIO_000300: 3.854e0

MQ
type: SiteQuality
SIO_000300: 4.821e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

QD
type: SiteQuality
SIO_000300: 6.6e0

MQRankSum
type: SiteQuality
SIO_000300: -2.054e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 9.67955e5

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26384
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4429
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3707
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2605
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4869
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4876
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.384e0

QD
type: SiteQuality
SIO_000300: 2.219e1

MQRankSum
type: SiteQuality
SIO_000300: -1.296e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.0738e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.239e0

GenotypeQuality
all individuals: 147
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
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GenotypeQuality
all individuals: 245
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4771
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2591
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4896
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.34e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 8.98498e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.556e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4719
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 333
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.593244642714889e-4
allele num: 25106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4733
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4857
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2570
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 1.717e0

QD
type: SiteQuality
SIO_000300: 1.656e1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 8.94266e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.355e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4615
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24797
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3557
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

MQ
type: SiteQuality
SIO_000300: 5.465e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.054e0

VQSLOD
type: SiteQuality
SIO_000300: -4.173e-1

QD
type: SiteQuality
SIO_000300: 7.7e-1

DP
type: SiteQuality
SIO_000300: 8.78572e5

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 317
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4407
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24077
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.385e1

MQ
type: SiteQuality
SIO_000300: 5.682e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.51e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.284e-1

DP
type: SiteQuality
SIO_000300: 8.55796e5

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4635
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3335
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4421
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2471
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.236245954692557e-3
allele num: 309
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

FS
type: SiteQuality
SIO_000300: 6.397e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.43429e5

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2417
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.391936404760859e-5
allele num: 22769
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4095
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3189
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

QD
type: SiteQuality
SIO_000300: 9.58e0

DP
type: SiteQuality
SIO_000300: 8.31502e5

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3414
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1142
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.801477211313277e-4
allele num: 22204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3890
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 5.079825834542816e-3
allele num: 4134
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 2.276348736626451e-4
allele num: 4393
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2378
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.719e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.2667e5

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

GenotypeQuality
all individuals: 4103
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 443
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2983
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.807569206580942e-5
allele num: 35618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7314
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5285
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 451
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

QD
type: SiteQuality
SIO_000300: 2.531e1

VQSLOD
type: SiteQuality
SIO_000300: -3.201e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.077769e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1030
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5685
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.601659858990036e-5
allele num: 38437
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7075
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.237927e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 2.87e1

GenotypeQuality
all individuals: 249
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3985
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8275
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3585
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40607
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.966679888932963e-4
allele num: 7563
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5919
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 2.422e0

DP
type: SiteQuality
SIO_000300: 1.324365e6