X-129790567-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790567
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790567
    reference: chr 0
allele count: 1
allele frequency: 1.204920896943116e-5
allele num: 82993
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1204A>G
  hgvsp: ENSP00000337146.3:p.Thr402Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1117A>G
  hgvsp: ENSP00000377890.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1117A>G
  hgvsp: ENSP00000400304.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1117A>G
  hgvsp: ENSP00000359973.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1204A>G
  hgvsp: ENSP00000359965.1:p.Thr402Ala
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr402Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-129790586-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790586
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790586
    reference: chr 0
allele count: 1
allele frequency: 1.17000117000117e-5
allele num: 85470
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1185A>T
  hgvsp: ENSP00000337146.3:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1098A>T
  hgvsp: ENSP00000377890.1:p.Glu366Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1185A>T
  hgvsp: ENSP00000359965.1:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1098A>T
  hgvsp: ENSP00000359973.1:p.Glu366Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1098A>T
  hgvsp: ENSP00000400304.1:p.Glu366Asp
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu395Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

X-129790598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790598
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790598
    reference: chr 0
allele count: 1
allele frequency: 1.158667995272635e-5
allele num: 86306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1086T>C
  hgvsp: ENST00000432489.1:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1173T>C
  hgvsp: ENST00000338144.3:c.1173T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1086T>C
  hgvsp: ENST00000394363.1:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1173T>C
  hgvsp: ENST00000370927.1:c.1173T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1086T>C
  hgvsp: ENST00000370935.1:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asp391Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

X-129790606-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790606
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790606
    reference: chr 0
allele count: 2
allele frequency: 2.31000231000231e-5
allele num: 86580
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1165T>G
  hgvsp: ENSP00000337146.3:p.Ser389Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1165T>G
  hgvsp: ENSP00000359965.1:p.Ser389Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1078T>G
  hgvsp: ENSP00000400304.1:p.Ser360Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1078T>G
  hgvsp: ENSP00000377890.1:p.Ser360Ala
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1078T>G
  hgvsp: ENSP00000359973.1:p.Ser360Ala
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
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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: 1269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser389Ala
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

X-129790622-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790622
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790622
    reference: chr 0
allele count: 1
allele frequency: 1.152937107280798e-5
allele num: 86735
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1062A>C
  hgvsp: ENSP00000400304.1:p.Glu354Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1062A>C
  hgvsp: ENSP00000377890.1:p.Glu354Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1149A>C
  hgvsp: ENSP00000359965.1:p.Glu383Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1149A>C
  hgvsp: ENSP00000337146.3:p.Glu383Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1062A>C
  hgvsp: ENSP00000359973.1:p.Glu354Asp
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38746
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 550
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 593
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
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genotype quality: GenotypeQuality
  all individuals: 153
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genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 30
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genotype quality: GenotypeQuality
  all individuals: 6078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43137
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu383Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-129790626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790626
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790626
    reference: chr 0
allele count: 1
allele frequency: 1.15304345820794e-5
allele num: 86727
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1145G>A
  hgvsp: ENSP00000337146.3:p.Arg382Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1145G>A
  hgvsp: ENSP00000359965.1:p.Arg382Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1058G>A
  hgvsp: ENSP00000377890.1:p.Arg353Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1058G>A
  hgvsp: ENSP00000359973.1:p.Arg353Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1058G>A
  hgvsp: ENSP00000400304.1:p.Arg353Gln
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
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genotype depth: GenotypeDepth
  all individuals: 512
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38602
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 167
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genotype quality: GenotypeQuality
  all individuals: 11
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42959
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genotype quality: GenotypeQuality
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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: 4162
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg382Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

X-129790651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790651
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790651
    reference: chr 0
allele count: 1
allele frequency: 1.158882836945185e-5
allele num: 86290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1033A>G
  hgvsp: ENSP00000359973.1:p.Asn345Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1120A>G
  hgvsp: ENSP00000359965.1:p.Asn374Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1033A>G
  hgvsp: ENSP00000400304.1:p.Asn345Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1120A>G
  hgvsp: ENSP00000337146.3:p.Asn374Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1033A>G
  hgvsp: ENSP00000377890.1:p.Asn345Asp
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37094
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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
  all individuals: 1074
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 45
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genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn374Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

X-129790658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790658
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790658
    reference: chr 0
allele count: 1
allele frequency: 1.164510381610052e-5
allele num: 85873
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1113C>T
  hgvsp: ENST00000370927.1:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1026C>T
  hgvsp: ENST00000370935.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1113C>T
  hgvsp: ENST00000338144.3:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1026C>T
  hgvsp: ENST00000394363.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1026C>T
  hgvsp: ENST00000432489.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35937
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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
  all individuals: 1739
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 429
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  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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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 665
  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6077
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn371Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

X-129790659-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790659
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790659
    reference: chr 0
allele count: 1
allele frequency: 1.165365342034728e-5
allele num: 85810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1112A>G
  hgvsp: ENSP00000359965.1:p.Asn371Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1025A>G
  hgvsp: ENSP00000400304.1:p.Asn342Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1025A>G
  hgvsp: ENSP00000377890.1:p.Asn342Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1025A>G
  hgvsp: ENSP00000359973.1:p.Asn342Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1112A>G
  hgvsp: ENSP00000337146.3:p.Asn371Ser
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 550
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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
  all individuals: 1318
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 429
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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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  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
  all individuals: 505
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn371Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

X-129790662-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790662
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790662
    reference: chr 0
allele count: 3
allele frequency: 3.506680225830207e-5
allele num: 85551
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1022G>A
  hgvsp: ENSP00000377890.1:p.Arg341His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1022G>A
  hgvsp: ENSP00000359973.1:p.Arg341His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1022G>A
  hgvsp: ENSP00000400304.1:p.Arg341His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1109G>A
  hgvsp: ENSP00000359965.1:p.Arg370His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1109G>A
  hgvsp: ENSP00000337146.3:p.Arg370His
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 274
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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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 198
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 10205
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 247
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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
  all individuals: 274
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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
  all individuals: 3570
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  variant carriers: 0
hgvs: p.Arg370His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

X-129790663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790663
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790663
    reference: chr 0
allele count: 2
allele frequency: 2.34000234000234e-5
allele num: 85470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1021C>T
  hgvsp: ENSP00000400304.1:p.Arg341Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1108C>T
  hgvsp: ENSP00000359965.1:p.Arg370Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1108C>T
  hgvsp: ENSP00000337146.3:p.Arg370Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1021C>T
  hgvsp: ENSP00000359973.1:p.Arg341Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1021C>T
  hgvsp: ENSP00000377890.1:p.Arg341Cys
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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
  all individuals: 349
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  variant carriers: 0
hgvs: p.Arg370Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

X-129790675-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790675
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790675
    reference: chr 0
allele count: 1
allele frequency: 1.185831683050908e-5
allele num: 84329
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-6C>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-6C>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-6C>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-6C>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-6C>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
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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: 550
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
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  variant carriers: 0
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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6166
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1102-6C>A
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

X-129790683-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790683
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790682
    reference: chr 0
allele count: 2
allele frequency: 2.39457867388233e-5
allele num: 83522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-15delA
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-15delA
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-15delA
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-15delA
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-15delA
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  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 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: 31101
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GT
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

X-129790698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790698
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790698
    reference: chr 0
allele count: 1
allele frequency: 1.218145495297958e-5
allele num: 82092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-29C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-29C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-29C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-29C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-29C>T
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
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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
  all individuals: 1052
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num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-129790700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790700
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790700
    reference: chr 0
allele count: 1
allele frequency: 1.224289911851126e-5
allele num: 81680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-31C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-31C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-31C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-31C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-31C>T
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
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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 quality: GenotypeQuality
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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: 560
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-129790703-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790703
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790703
    reference: chr 0
allele count: 1
allele frequency: 1.224020171852432e-5
allele num: 81698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-34A>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-34A>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-34A>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-34A>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-34A>C
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 6070
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

X-129790705-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790705
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790705
    reference: chr 0
allele count: 1
allele frequency: 1.22845595371178e-5
allele num: 81403
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-36G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-36G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-36G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-36G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-36G>T
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

X-129790706-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129790706
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129790706
    reference: chr 0
allele count: 1
allele frequency: 1.229951785889993e-5
allele num: 81304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1015-37G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1015-37G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1015-37G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1102-37G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1102-37G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

X-129799568-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799568
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799568
    reference: chr 0
allele count: 1
allele frequency: 5.177323323841574e-5
allele num: 19315
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+49G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+49G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+49G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+49G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+49G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-129799569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799569
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799569
    reference: chr 0
allele count: 1
allele frequency: 5.153045449860868e-5
allele num: 19406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+48C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+48C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+48C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+48C>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+48C>T
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
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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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  variant carriers: 0
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 quality: GenotypeQuality
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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: 2.75e1
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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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  bin: 2.25e1
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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: 4.75e1
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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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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

X-129799580-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799580
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799581
    reference: chr 0
allele count: 2
allele frequency: 1.007455168245013e-4
allele num: 19852
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+36dupG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+36dupG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+36dupG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+36dupG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+36dupG
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17637
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 197
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2780
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genotype quality: GenotypeQuality
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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: 335
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genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

X-129799580-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799580
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799579
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 19852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+36delG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+36delG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+36delG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+36delG
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+36delG
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 131
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: TC
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

X-129799581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799581
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799581
    reference: chr 0
allele count: 1
allele frequency: 5.02209722780233e-5
allele num: 19912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+36G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+36G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+36G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+36G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+36G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
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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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num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

X-129799583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799583
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799583
    reference: chr 0
allele count: 2
allele frequency: 9.822217856792063e-5
allele num: 20362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+34G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+34G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+34G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+34G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+34G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  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
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genotype depth: GenotypeDepth
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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: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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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: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

X-129799584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799584
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799584
    reference: chr 0
allele count: 1
allele frequency: 4.874482086278333e-5
allele num: 20515
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+33G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+33G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+33G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+33G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+33G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1921
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

X-129799585-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799585
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799585
    reference: chr 0
allele count: 1
allele frequency: 4.836057645807138e-5
allele num: 20678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+32G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+32G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+32G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+32G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+32G>T
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

X-129799585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799585
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799585
    reference: chr 0
allele count: 7
allele frequency: 3.385240352064996e-4
allele num: 20678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+32G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+32G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+32G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+32G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+32G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
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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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num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
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site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-129799587-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799587
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799587
    reference: chr 0
allele count: 75
allele frequency: 3.563961224101882e-3
allele num: 21044
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+30T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+30T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+30T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+30T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+30T>C
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 3
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: 7.75e1
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

X-129799596-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799596
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799596
    reference: chr 0
allele count: 1
allele frequency: 4.348204191668841e-5
allele num: 22998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+21G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+21G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+21G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+21G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+21G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 22456
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

X-129799599-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799599
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799599
    reference: chr 0
allele count: 1
allele frequency: 4.163544008660171e-5
allele num: 24018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+18C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+18C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+18C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+18C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+18C>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 180
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

X-129799600-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799600
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799600
    reference: chr 0
allele count: 1
allele frequency: 4.08730483119431e-5
allele num: 24466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+17T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+17T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+17T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+17T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+17T>C
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

X-129799602-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799602
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799602
    reference: chr 0
allele count: 1
allele frequency: 3.984381225595665e-5
allele num: 25098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+15A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+15A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+15A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+15A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+15A>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  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 quality: GenotypeQuality
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  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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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1909
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15862
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS

X-129799608-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799608
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799608
    reference: chr 0
allele count: 1
allele frequency: 3.691126531817511e-5
allele num: 27092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1014+9C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1101+9C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1101+9C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1014+9C>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1014+9C>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28778
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 139
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genotype depth: GenotypeDepth
  all individuals: 245
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 141
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  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
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13787
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-129799619-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799619
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799619
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 34506
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1099G>C
  hgvsp: ENSP00000337146.3:p.Glu367Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1012G>C
  hgvsp: ENSP00000400304.1:p.Glu338Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1012G>C
  hgvsp: ENSP00000359973.1:p.Glu338Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1012G>C
  hgvsp: ENSP00000377890.1:p.Glu338Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1099G>C
  hgvsp: ENSP00000359965.1:p.Glu367Gln
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
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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: 9.25e1
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genotype depth: GenotypeDepth
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  bin: 7.25e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 496
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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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  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
  all individuals: 1120
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu367Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

X-129799619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799619
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799619
    reference: chr 0
allele count: 6
allele frequency: 1.738828029907842e-4
allele num: 34506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.1012G>A
  hgvsp: ENSP00000400304.1:p.Glu338Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1099G>A
  hgvsp: ENSP00000359965.1:p.Glu367Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1099G>A
  hgvsp: ENSP00000337146.3:p.Glu367Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.1012G>A
  hgvsp: ENSP00000377890.1:p.Glu338Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.1012G>A
  hgvsp: ENSP00000359973.1:p.Glu338Lys
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 2.25e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 28849
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu367Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

X-129799632-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799632
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799632
    reference: chr 0
allele count: 1
allele frequency: 2.300595854326271e-5
allele num: 43467
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.999G>C
  hgvsp: ENSP00000377890.1:p.Trp333Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.999G>C
  hgvsp: ENSP00000359973.1:p.Trp333Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.999G>C
  hgvsp: ENSP00000400304.1:p.Trp333Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1086G>C
  hgvsp: ENSP00000337146.3:p.Trp362Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1086G>C
  hgvsp: ENSP00000359965.1:p.Trp362Cys
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28645
  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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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 16049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5637
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 927
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Trp362Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

X-129799632-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799632
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799632
    reference: chr 0
allele count: 1
allele frequency: 2.300595854326271e-5
allele num: 43467
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.999G>A
  hgvsp: ENSP00000400304.1:p.Trp333Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.999G>A
  hgvsp: ENSP00000377890.1:p.Trp333Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.999G>A
  hgvsp: ENSP00000359973.1:p.Trp333Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1086G>A
  hgvsp: ENSP00000337146.3:p.Trp362Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1086G>A
  hgvsp: ENSP00000359965.1:p.Trp362Ter
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28645
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
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genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
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genotype depth: GenotypeDepth
  all individuals: 245
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genotype quality: GenotypeQuality
  all individuals: 5637
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 219
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genotype quality: GenotypeQuality
  all individuals: 341
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genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
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genotype quality: GenotypeQuality
  all individuals: 16756
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 436
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27906
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genotype quality: GenotypeQuality
  all individuals: 250
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Trp362Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

X-129799637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799637
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799637
    reference: chr 0
allele count: 1
allele frequency: 2.179456443562975e-5
allele num: 45883
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.994G>A
  hgvsp: ENSP00000377890.1:p.Val332Met
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1081G>A
  hgvsp: ENSP00000337146.3:p.Val361Met
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.994G>A
  hgvsp: ENSP00000359973.1:p.Val332Met
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.994G>A
  hgvsp: ENSP00000400304.1:p.Val332Met
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1081G>A
  hgvsp: ENSP00000359965.1:p.Val361Met
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
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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: 0
genotype depth: GenotypeDepth
  all individuals: 27938
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 193
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1910
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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: 402
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 440
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genotype quality: GenotypeQuality
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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: 516
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val361Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

X-129799638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799638
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799638
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 46687
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.993C>T
  hgvsp: ENST00000370935.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.993C>T
  hgvsp: ENST00000432489.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1080C>T
  hgvsp: ENST00000338144.3:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1080C>T
  hgvsp: ENST00000370927.1:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.993C>T
  hgvsp: ENST00000394363.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27653
  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 depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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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  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: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 27022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser360Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

X-129799668-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799668
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799668
    reference: chr 0
allele count: 2
allele frequency: 3.60366853456819e-5
allele num: 55499
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.963C>T
  hgvsp: ENST00000394363.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.963C>T
  hgvsp: ENST00000370935.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.963C>T
  hgvsp: ENST00000432489.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1050C>T
  hgvsp: ENST00000338144.3:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1050C>T
  hgvsp: ENST00000370927.1:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21372
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22454
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His350His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-129799671-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799671
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799671
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 55819
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1047C>A
  hgvsp: ENSP00000359965.1:p.Asp349Glu
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.960C>A
  hgvsp: ENSP00000359973.1:p.Asp320Glu
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1047C>A
  hgvsp: ENSP00000337146.3:p.Asp349Glu
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.960C>A
  hgvsp: ENSP00000377890.1:p.Asp320Glu
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.960C>A
  hgvsp: ENSP00000400304.1:p.Asp320Glu
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 1.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 72
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genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 1911
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 382
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2999
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp349Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

X-129799671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799671
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799671
    reference: chr 0
allele count: 1
allele frequency: 1.791504684784751e-5
allele num: 55819
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.960C>T
  hgvsp: ENST00000370935.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.960C>T
  hgvsp: ENST00000432489.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.960C>T
  hgvsp: ENST00000394363.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1047C>T
  hgvsp: ENST00000370927.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1047C>T
  hgvsp: ENST00000338144.3:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 382
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
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genotype quality: GenotypeQuality
  all individuals: 24457
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genotype quality: GenotypeQuality
  all individuals: 740
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 2999
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp349Asp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-129799682-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799682
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799682
    reference: chr 0
allele count: 2
allele frequency: 3.575706649026514e-5
allele num: 55933
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1036A>C
  hgvsp: ENSP00000359965.1:p.Lys346Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.949A>C
  hgvsp: ENSP00000400304.1:p.Lys317Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.949A>C
  hgvsp: ENSP00000377890.1:p.Lys317Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.949A>C
  hgvsp: ENSP00000359973.1:p.Lys317Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1036A>C
  hgvsp: ENSP00000337146.3:p.Lys346Gln
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23283
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 3.25e1
  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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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 141
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1912
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys346Gln
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

X-129799694-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799694
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799694
    reference: chr 0
allele count: 2
allele frequency: 3.704115272067267e-5
allele num: 53994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.937G>T
  hgvsp: ENSP00000377890.1:p.Ala313Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.937G>T
  hgvsp: ENSP00000400304.1:p.Ala313Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1024G>T
  hgvsp: ENSP00000359965.1:p.Ala342Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1024G>T
  hgvsp: ENSP00000337146.3:p.Ala342Ser
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.937G>T
  hgvsp: ENSP00000359973.1:p.Ala313Ser
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18065
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 1
hgvs: p.Ala342Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-129799694-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799694
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799694
    reference: chr 0
allele count: 10
allele frequency: 1.852057636033633e-4
allele num: 53994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.937G>A
  hgvsp: ENSP00000377890.1:p.Ala313Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1024G>A
  hgvsp: ENSP00000337146.3:p.Ala342Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1024G>A
  hgvsp: ENSP00000359965.1:p.Ala342Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.937G>A
  hgvsp: ENSP00000400304.1:p.Ala313Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.937G>A
  hgvsp: ENSP00000359973.1:p.Ala313Thr
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23433
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24814
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18065
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala342Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-129799695-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799695
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799695
    reference: chr 0
allele count: 2
allele frequency: 3.701784260013326e-5
allele num: 54028
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1023C>T
  hgvsp: ENST00000338144.3:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.936C>T
  hgvsp: ENST00000432489.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.936C>T
  hgvsp: ENST00000394363.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.936C>T
  hgvsp: ENST00000370935.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1023C>T
  hgvsp: ENST00000370927.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23445
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4244
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 391
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1911
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
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genotype quality: GenotypeQuality
  all individuals: 198
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genotype quality: GenotypeQuality
  all individuals: 545
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genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser341Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

X-129799699-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799699
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799699
    reference: chr 0
allele count: 2
allele frequency: 3.739925575481048e-5
allele num: 53477
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1019A>C
  hgvsp: ENSP00000337146.3:p.His340Pro
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.932A>C
  hgvsp: ENSP00000400304.1:p.His311Pro
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.932A>C
  hgvsp: ENSP00000377890.1:p.His311Pro
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1019A>C
  hgvsp: ENSP00000359965.1:p.His340Pro
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.932A>C
  hgvsp: ENSP00000359973.1:p.His311Pro
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His340Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

X-129799701-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799701
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799701
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 52971
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.930C>A
  hgvsp: ENSP00000400304.1:p.Tyr310Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1017C>A
  hgvsp: ENSP00000359965.1:p.Tyr339Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.930C>A
  hgvsp: ENSP00000359973.1:p.Tyr310Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1017C>A
  hgvsp: ENSP00000337146.3:p.Tyr339Ter
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.930C>A
  hgvsp: ENSP00000377890.1:p.Tyr310Ter
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: stop gained
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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  bin: 2.25e1
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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: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
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genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 103
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 25382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr339Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

X-129799702-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799702
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799702
    reference: chr 0
allele count: 1
allele frequency: 1.894872475082427e-5
allele num: 52774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1016A>T
  hgvsp: ENSP00000359965.1:p.Tyr339Phe
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.929A>T
  hgvsp: ENSP00000400304.1:p.Tyr310Phe
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.929A>T
  hgvsp: ENSP00000359973.1:p.Tyr310Phe
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1016A>T
  hgvsp: ENSP00000337146.3:p.Tyr339Phe
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.929A>T
  hgvsp: ENSP00000377890.1:p.Tyr310Phe
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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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  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
  all individuals: 1303
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17240
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr339Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

X-129799703-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799703
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799703
    reference: chr 0
allele count: 2
allele frequency: 3.803365978891319e-5
allele num: 52585
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.928T>G
  hgvsp: ENSP00000400304.1:p.Tyr310Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.928T>G
  hgvsp: ENSP00000359973.1:p.Tyr310Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1015T>G
  hgvsp: ENSP00000359965.1:p.Tyr339Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.928T>G
  hgvsp: ENSP00000377890.1:p.Tyr310Asp
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1015T>G
  hgvsp: ENSP00000337146.3:p.Tyr339Asp
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 927
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr339Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum

X-129799705-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799705
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799705
    reference: chr 0
allele count: 833
allele frequency: 1.663870246085011e-2
allele num: 50064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.1013T>G
  hgvsp: ENSP00000359965.1:p.Val338Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.926T>G
  hgvsp: ENSP00000377890.1:p.Val309Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.926T>G
  hgvsp: ENSP00000400304.1:p.Val309Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.926T>G
  hgvsp: ENSP00000359973.1:p.Val309Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.1013T>G
  hgvsp: ENSP00000337146.3:p.Val338Gly
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 119
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 5.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 28
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 9.75e1
  variant carriers: 678
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 7.5e0
  variant carriers: 10
hgvs: p.Val338Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-129799721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799721
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799721
    reference: chr 0
allele count: 1
allele frequency: 2.023922767107207e-5
allele num: 49409
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.910G>A
  hgvsp: ENSP00000359973.1:p.Glu304Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.910G>A
  hgvsp: ENSP00000377890.1:p.Glu304Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.910G>A
  hgvsp: ENSP00000400304.1:p.Glu304Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.997G>A
  hgvsp: ENSP00000337146.3:p.Glu333Lys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.997G>A
  hgvsp: ENSP00000359965.1:p.Glu333Lys
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12982
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7718
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu333Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD

X-129799727-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799727
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799727
    reference: chr 0
allele count: 1
allele frequency: 2.076067098488623e-5
allele num: 48168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.995-4G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.908-4G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.908-4G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.908-4G>T
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.995-4G>T
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22315
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
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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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  bin: 6.25e1
  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
  all individuals: 1211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27136
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
hgvs: c.995-4G>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

X-129799736-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799736
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799736
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 45946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.908-13T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.908-13T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.995-13T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.908-13T>C
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.995-13T>C
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 1.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

X-129799748-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799748
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799748
    reference: chr 0
allele count: 1
allele frequency: 2.348244687096396e-5
allele num: 42585
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.995-25T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.995-25T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.908-25T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.908-25T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.908-25T>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19675
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
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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
  all individuals: 610
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2047
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 356
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

X-129799749-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799749
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799749
    reference: chr 0
allele count: 1
allele frequency: 2.363842662632375e-5
allele num: 42304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.995-26A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.908-26A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.908-26A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.995-26A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.908-26A>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 2.75e1
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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: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 15157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-129799750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799750
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799750
    reference: chr 0
allele count: 1
allele frequency: 2.388344877000239e-5
allele num: 41870
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.995-27G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.995-27G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.908-27G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.908-27G>A
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.908-27G>A
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

X-129799765-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129799765
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129799765
    reference: chr 0
allele count: 116
allele frequency: 3.172172391161671e-3
allele num: 36568
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.995-42A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.908-42A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.908-42A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.908-42A>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.995-42A>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 1986
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  variant carriers: 108
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

X-129801456-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801456
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801456
    reference: chr 0
allele count: 1
allele frequency: 1.163345315790086e-5
allele num: 85959
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.907+48T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.907+48T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.994+48T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.994+48T>G
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.907+48T>G
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22893
  bin: 2.75e1
  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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  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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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: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-129801511-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801511
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801511
    reference: chr 0
allele count: 3
allele frequency: 3.427357164890153e-5
allele num: 87531
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.900C>A
  hgvsp: ENST00000394363.1:c.900C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.900C>A
  hgvsp: ENST00000432489.1:c.900C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.987C>A
  hgvsp: ENST00000338144.3:c.987C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.987C>A
  hgvsp: ENST00000370927.1:c.987C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.900C>A
  hgvsp: ENST00000370935.1:c.900C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9552
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu329Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

X-129801525-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801525
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801525
    reference: chr 0
allele count: 1
allele frequency: 1.140081857877396e-5
allele num: 87713
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.973C>A
  hgvsp: ENSP00000337146.3:p.Leu325Ile
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.886C>A
  hgvsp: ENSP00000359973.1:p.Leu296Ile
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.886C>A
  hgvsp: ENSP00000400304.1:p.Leu296Ile
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.886C>A
  hgvsp: ENSP00000377890.1:p.Leu296Ile
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.973C>A
  hgvsp: ENSP00000359965.1:p.Leu325Ile
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9593
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu325Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-129801532-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801532
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801532
    reference: chr 0
allele count: 1
allele frequency: 1.139692055206683e-5
allele num: 87743
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.966G>C
  hgvsp: ENSP00000359965.1:p.Lys322Asn
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.879G>C
  hgvsp: ENSP00000359973.1:p.Lys293Asn
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.879G>C
  hgvsp: ENSP00000377890.1:p.Lys293Asn
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.879G>C
  hgvsp: ENSP00000400304.1:p.Lys293Asn
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.966G>C
  hgvsp: ENSP00000337146.3:p.Lys322Asn
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44594
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9599
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys322Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

X-129801548-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801548
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801548
    reference: chr 0
allele count: 3
allele frequency: 3.418491761434855e-5
allele num: 87758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.863C>G
  hgvsp: ENSP00000359973.1:p.Ala288Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.950C>G
  hgvsp: ENSP00000337146.3:p.Ala317Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.863C>G
  hgvsp: ENSP00000377890.1:p.Ala288Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.863C>G
  hgvsp: ENSP00000400304.1:p.Ala288Gly
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.950C>G
  hgvsp: ENSP00000359965.1:p.Ala317Gly
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9606
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala317Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

X-129801557-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801557
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801557
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.854T>C
  hgvsp: ENSP00000359973.1:p.Met285Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.941T>C
  hgvsp: ENSP00000359965.1:p.Met314Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.941T>C
  hgvsp: ENSP00000337146.3:p.Met314Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.854T>C
  hgvsp: ENSP00000400304.1:p.Met285Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.854T>C
  hgvsp: ENSP00000377890.1:p.Met285Thr
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18405
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 44649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
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genotype quality: GenotypeQuality
  all individuals: 5
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9607
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met314Thr
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: A
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-129801563-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801563
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801563
    reference: chr 0
allele count: 1
allele frequency: 1.139445318019188e-5
allele num: 87762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.935A>C
  hgvsp: ENSP00000359965.1:p.Lys312Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.935A>C
  hgvsp: ENSP00000337146.3:p.Lys312Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.848A>C
  hgvsp: ENSP00000359973.1:p.Lys283Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.848A>C
  hgvsp: ENSP00000400304.1:p.Lys283Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.848A>C
  hgvsp: ENSP00000377890.1:p.Lys283Thr
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
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genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
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genotype depth: GenotypeDepth
  all individuals: 73
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18404
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
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genotype quality: GenotypeQuality
  all individuals: 270
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1698
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genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys312Thr
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

X-129801567-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801567
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801567
    reference: chr 0
allele count: 2
allele frequency: 2.278864669621595e-5
allele num: 87763
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.844G>C
  hgvsp: ENSP00000400304.1:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.931G>C
  hgvsp: ENSP00000359965.1:p.Glu311Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.931G>C
  hgvsp: ENSP00000337146.3:p.Glu311Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.844G>C
  hgvsp: ENSP00000377890.1:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.844G>C
  hgvsp: ENSP00000359973.1:p.Glu282Gln
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 2
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: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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
genotype quality: GenotypeQuality
  all individuals: 1697
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
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  variant carriers: 0
hgvs: p.Glu311Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

X-129801576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801576
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801576
    reference: chr 0
allele count: 1
allele frequency: 1.139445318019188e-5
allele num: 87762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.835G>A
  hgvsp: ENSP00000400304.1:p.Ala279Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.922G>A
  hgvsp: ENSP00000337146.3:p.Ala308Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.922G>A
  hgvsp: ENSP00000359965.1:p.Ala308Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.835G>A
  hgvsp: ENSP00000377890.1:p.Ala279Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.835G>A
  hgvsp: ENSP00000359973.1:p.Ala279Thr
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8412
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
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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
  all individuals: 6081
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  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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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
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: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala308Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

X-129801583-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801583
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801583
    reference: chr 0
allele count: 3
allele frequency: 3.418413855970829e-5
allele num: 87760
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.915C>T
  hgvsp: ENST00000338144.3:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.828C>T
  hgvsp: ENST00000370935.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.915C>T
  hgvsp: ENST00000370927.1:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.828C>T
  hgvsp: ENST00000394363.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.828C>T
  hgvsp: ENST00000432489.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 45
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 644
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genotype depth: GenotypeDepth
  all individuals: 86
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 176
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genotype depth: GenotypeDepth
  all individuals: 294
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn305Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

X-129801593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801593
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801593
    reference: chr 0
allele count: 6
allele frequency: 6.836827711941659e-5
allele num: 87760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.818G>A
  hgvsp: ENSP00000400304.1:p.Arg273His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.905G>A
  hgvsp: ENSP00000337146.3:p.Arg302His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.818G>A
  hgvsp: ENSP00000377890.1:p.Arg273His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.818G>A
  hgvsp: ENSP00000359973.1:p.Arg273His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.905G>A
  hgvsp: ENSP00000359965.1:p.Arg302His
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8404
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 176
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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genotype depth: GenotypeDepth
  all individuals: 71
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 6083
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg302His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

X-129801594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801594
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801594
    reference: chr 0
allele count: 3
allele frequency: 3.418491761434855e-5
allele num: 87758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.817C>T
  hgvsp: ENSP00000377890.1:p.Arg273Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.904C>T
  hgvsp: ENSP00000337146.3:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.904C>T
  hgvsp: ENSP00000359965.1:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.817C>T
  hgvsp: ENSP00000359973.1:p.Arg273Cys
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.817C>T
  hgvsp: ENSP00000400304.1:p.Arg273Cys
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1
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  variant carriers: 0
hgvs: p.Arg302Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-129801596-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801596
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801596
    reference: chr 0
allele count: 2
allele frequency: 2.279020476998986e-5
allele num: 87757
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.815G>A
  hgvsp: ENSP00000400304.1:p.Arg272His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.815G>A
  hgvsp: ENSP00000359973.1:p.Arg272His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.902G>A
  hgvsp: ENSP00000359965.1:p.Arg301His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.902G>A
  hgvsp: ENSP00000337146.3:p.Arg301His
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.815G>A
  hgvsp: ENSP00000377890.1:p.Arg272His
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24030
  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg301His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

X-129801598-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801598
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801598
    reference: chr 0
allele count: 8
allele frequency: 9.115874155357286e-5
allele num: 87759
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.900C>A
  hgvsp: ENST00000338144.3:c.900C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.813C>A
  hgvsp: ENST00000432489.1:c.813C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.813C>A
  hgvsp: ENST00000370935.1:c.813C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.813C>A
  hgvsp: ENST00000394363.1:c.813C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.900C>A
  hgvsp: ENST00000370927.1:c.900C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44655
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val300Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

X-129801608-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801608
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801608
    reference: chr 0
allele count: 1
allele frequency: 1.139588152841563e-5
allele num: 87751
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.890A>C
  hgvsp: ENSP00000359965.1:p.Asn297Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.803A>C
  hgvsp: ENSP00000377890.1:p.Asn268Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.803A>C
  hgvsp: ENSP00000400304.1:p.Asn268Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.890A>C
  hgvsp: ENSP00000337146.3:p.Asn297Thr
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.803A>C
  hgvsp: ENSP00000359973.1:p.Asn268Thr
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24045
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9612
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn297Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

X-129801613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24129801613
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24129801613
    reference: chr 0
allele count: 7
allele frequency: 7.97620811066419e-5
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000377890
  ensembl transcript: ENST00000394363
  gene symbol: ENOX2
  hgvsc: ENST00000394363.1:c.798G>A
  hgvsp: ENST00000394363.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359973
  ensembl transcript: ENST00000370935
  gene symbol: ENOX2
  hgvsc: ENST00000370935.1:c.798G>A
  hgvsp: ENST00000370935.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000400304
  ensembl transcript: ENST00000432489
  gene symbol: ENOX2
  hgvsc: ENST00000432489.1:c.798G>A
  hgvsp: ENST00000432489.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000359965
  ensembl transcript: ENST00000370927
  gene symbol: ENOX2
  hgvsc: ENST00000370927.1:c.885G>A
  hgvsp: ENST00000370927.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165675
  ensembl protein: ENSP00000337146
  ensembl transcript: ENST00000338144
  gene symbol: ENOX2
  hgvsc: ENST00000338144.3:c.885G>A
  hgvsp: ENST00000338144.3:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2259
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser295Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6078
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8391
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4463
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.215379162143601e-5
allele num: 45139
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-2

DP
type: SiteQuality
SIO_000300: 1.680094e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

GenotypeQuality
all individuals: 176
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6078
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46744
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8449
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9213
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.227e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.333e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.203e0

QD
type: SiteQuality
SIO_000300: 1.208e1

DP
type: SiteQuality
SIO_000300: 1.728339e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.115238175818597e-5
allele num: 47276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6585
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.745192e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.155e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.15e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.247e0

QD
type: SiteQuality
SIO_000300: 2.813e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 506
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47417
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6601
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.062068254459223e-4
allele num: 9699
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.868e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.751349e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.35e-2

QD
type: SiteQuality
SIO_000300: 3.115e1

VQSLOD
type: SiteQuality
SIO_000300: -4.025e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1175
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GenotypeQuality
all individuals: 1333
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8465
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9767
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.105928187848794e-5
allele num: 47485
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 1.75478e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -5.059e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.833e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

GenotypeQuality
all individuals: 144
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variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1330
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variant carriers: 0

GenotypeQuality
all individuals: 1551
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6603
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.106238678967101e-5
allele num: 47478
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.633e0

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 8.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 3.849e0

DP
type: SiteQuality
SIO_000300: 1.755021e6

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
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variant carriers: 0

GenotypeQuality
all individuals: 1317
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GenotypeQuality
all individuals: 4110
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variant carriers: 0

GenotypeQuality
all individuals: 95
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GenotypeQuality
all individuals: 334
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Finnish)
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: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.122331168555541e-5
allele num: 47118
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9763
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.746e0

QD
type: SiteQuality
SIO_000300: 1.761e1

VQSLOD
type: SiteQuality
SIO_000300: -1.463e0

DP
type: SiteQuality
SIO_000300: 1.742132e6

GenotypeQuality
all individuals: 505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
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variant carriers: 0

GenotypeQuality
all individuals: 1306
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variant carriers: 0

GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4505
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9719
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8435
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.136158759318993e-5
allele num: 46813
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.728452e6

VQSLOD
type: SiteQuality
SIO_000300: -8.407e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.218e0

QD
type: SiteQuality
SIO_000300: 1.907e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.01e-2

FS
type: SiteQuality
SIO_000300: 4.544e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 5.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1515
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GenotypeQuality
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GenotypeQuality
all individuals: 6077
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GenotypeQuality
all individuals: 40373
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6567
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.138397057565649e-5
allele num: 46764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9717
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.725657e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: -1.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

FS
type: SiteQuality
SIO_000300: 2.213e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.371e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 228
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6077
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variant carriers: 3

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4497
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.292674550878925e-5
allele num: 46591
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.032524522457408e-4
allele num: 9685
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.28e-2

QD
type: SiteQuality
SIO_000300: 1.634e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

DP
type: SiteQuality
SIO_000300: 1.717677e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.032844453625284e-4
allele num: 9682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.149197274817855e-5
allele num: 46529
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8415
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.68e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e0

DP
type: SiteQuality
SIO_000300: 1.714273e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 348
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GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.544163063619518e-4
allele num: 6476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4467
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

DP
type: SiteQuality
SIO_000300: 1.667177e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

FS
type: SiteQuality
SIO_000300: 4.461e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.07e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 296
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GenotypeQuality
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GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.099517111064455e-4
allele num: 9526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8300
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9025
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45221
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.356e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.143e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.621808e6

MQ
type: SiteQuality
SIO_000300: 6.065e1

GenotypeQuality
all individuals: 248
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4410
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 591
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.217730150998539e-4
allele num: 8212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8915
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44268
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.052e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.84e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.54153e6

GenotypeQuality
all individuals: 4892
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9377
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43973
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8878
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.222045704509349e-4
allele num: 8183
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6257
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

DP
type: SiteQuality
SIO_000300: 1.524742e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.986e0

VQSLOD
type: SiteQuality
SIO_000300: -1.617e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

FS
type: SiteQuality
SIO_000300: 1.1706e1

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.078e0

QD
type: SiteQuality
SIO_000300: 1.271e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.81e-1

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3297
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8883
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.597699312989295e-4
allele num: 6259
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9370
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.431e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

DP
type: SiteQuality
SIO_000300: 1.520814e6

MQRankSum
type: SiteQuality
SIO_000300: 2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.45e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 591
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6239
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.283522104493971e-5
allele num: 43792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8167
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.513745e6

QD
type: SiteQuality
SIO_000300: 7.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.42e-1

GenotypeQuality
all individuals: 9342
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6070
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.287387346173201e-5
allele num: 43718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9343
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 3.142e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 1.510038e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
all individuals: 1919
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 9.182736455463728e-4
allele num: 1089
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 175
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9601
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 235
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 767
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 5.00417e5

QD
type: SiteQuality
SIO_000300: 9.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.17e-2

GenotypeQuality
all individuals: 1125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 771
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1087
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 175
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 235
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.03950103950104e-4
allele num: 9620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.01e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.27e-1

DP
type: SiteQuality
SIO_000300: 5.03637e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

VQSLOD
type: SiteQuality
SIO_000300: -8.265e-1

GenotypeQuality
all individuals: 3193
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 741
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
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GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 249
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 845
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.040191778027134e-4
allele num: 9803
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 175
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.909999999999999e-2

DP
type: SiteQuality
SIO_000300: 5.35119e5

QD
type: SiteQuality
SIO_000300: 1.074e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 175
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3052
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 845
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 249
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9803
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

FS
type: SiteQuality
SIO_000300: 7.43e-1

DP
type: SiteQuality
SIO_000300: 5.35119e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.909999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.074e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

GenotypeQuality
all individuals: 190
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1156
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 3.275466754012447e-4
allele num: 3053
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 173
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 2.012e1

DP
type: SiteQuality
SIO_000300: 5.39162e5

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 800
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GenotypeQuality
all individuals: 193
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1179
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 271
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 177
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 4.288164665523156e-4
allele num: 4664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10053
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.29e-2

FS
type: SiteQuality
SIO_000300: 7.335e0

QD
type: SiteQuality
SIO_000300: 1.22e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 5.47928e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.784e-1

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 865
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10121
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 928
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 8.216926869350862e-4
allele num: 1217
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3121
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 6.298e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.52978e5

VQSLOD
type: SiteQuality
SIO_000300: -1.921e0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e0

QD
type: SiteQuality
SIO_000300: 1.851e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.26e-2

GenotypeQuality
all individuals: 1560
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
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variant carriers: 1

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4683
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.898894154818325e-4
allele num: 1266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 271
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10189
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3137
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.725e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 1.691e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.429999999999999e-2

DP
type: SiteQuality
SIO_000300: 5.57809e5

GenotypeQuality
all individuals: 3867
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 271
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10189
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 2.231431303793433e-3
allele num: 3137
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4683
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1266
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.725e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.429999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

DP
type: SiteQuality
SIO_000300: 5.57809e5

QD
type: SiteQuality
SIO_000300: 1.691e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

GenotypeQuality
all individuals: 1913
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1966
bin: 9.75e1
variant carriers: 68

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

African
type: Population
allele count: 70
allele frequency: 2.179327521793275e-2
allele num: 3212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.687106461300009e-5
allele num: 10323
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.044489383215369e-3
allele num: 989
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1317
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4731
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.89e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 7.88e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

DP
type: SiteQuality
SIO_000300: 5.70234e5

GenotypeQuality
all individuals: 644
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 484
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1551
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4955
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.880184331797235e-4
allele num: 3472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1264
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.322e0

MQRankSum
type: SiteQuality
SIO_000300: -8.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

DP
type: SiteQuality
SIO_000300: 6.1946e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.37e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.845e1

QD
type: SiteQuality
SIO_000300: 7.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

GenotypeQuality
all individuals: 257
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variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23731
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variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.983339944466482e-4
allele num: 5042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 205
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1659
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.38581e5

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.663e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 2.871e1

FS
type: SiteQuality
SIO_000300: 1.3277e1

VQSLOD
type: SiteQuality
SIO_000300: -1.302e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeQuality
all individuals: 497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
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variant carriers: 0

GenotypeQuality
all individuals: 16758
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variant carriers: 0

GenotypeQuality
all individuals: 6424
bin: 6.25e1
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GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11921
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.793742757821553e-4
allele num: 1726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1481
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5086
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.43482e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.234e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 5.677e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.623e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.28e0

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.96e-2

GenotypeQuality
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 25168
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variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12216
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.938735944164405e-4
allele num: 5158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1583
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 463
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.55402e5

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.88e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1909
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 126
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GenotypeQuality
all individuals: 407
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1905
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.579313902501935e-4
allele num: 3877
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

DP
type: SiteQuality
SIO_000300: 6.87545e5

VQSLOD
type: SiteQuality
SIO_000300: -2.683e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.55e-2

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

FS
type: SiteQuality
SIO_000300: 8.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 172
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GenotypeQuality
all individuals: 1222
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 386
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GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2849
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16925
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3305
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

QD
type: SiteQuality
SIO_000300: 1.573e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 7.78944e5

FS
type: SiteQuality
SIO_000300: 4.817e0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 1090
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9051
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1914
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variant carriers: 4

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
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variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16925
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 1.815431164901664e-3
allele num: 3305
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2849
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

FS
type: SiteQuality
SIO_000300: 4.817e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

DP
type: SiteQuality
SIO_000300: 7.78944e5

QD
type: SiteQuality
SIO_000300: 1.573e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

GenotypeQuality
all individuals: 1910
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 436
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GenotypeQuality
all individuals: 259
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 293
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1239
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 21632
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3916
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.079002079002079e-4
allele num: 4810
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.395e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 9.121e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

DP
type: SiteQuality
SIO_000300: 8.75262e5

GenotypeQuality
all individuals: 545
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variant carriers: 0

GenotypeQuality
all individuals: 201
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GenotypeQuality
all individuals: 1407
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GenotypeQuality
all individuals: 280
bin: 4.75e1
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GenotypeQuality
all individuals: 258
bin: 5.75e1
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GenotypeQuality
all individuals: 486
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 21632
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: 4810
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.864628006712661e-4
allele num: 5363
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 293
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1239
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

DP
type: SiteQuality
SIO_000300: 8.75262e5

FS
type: SiteQuality
SIO_000300: 9.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4199
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.576292559899117e-4
allele num: 6344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 309
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5570
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5127
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22996
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

FS
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SIO_000300: 6.821e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

DP
type: SiteQuality
SIO_000300: 9.00868e5

VQSLOD
type: SiteQuality
SIO_000300: 2.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
SIO_000300: 9.15e0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6385
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5261
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4277
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.621e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: -2.739e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.754e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.286e0

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

African
type: Population
allele count: 2
allele frequency: 3.178639542275906e-4
allele num: 6292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5029
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1835
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28715
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6421
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6829
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.443e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 9.99046e5

VQSLOD
type: SiteQuality
SIO_000300: -1.622e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 2.799e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 740
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6463
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5059
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1843
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.028e0

QD
type: SiteQuality
SIO_000300: 8.84e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.03e-1

DP
type: SiteQuality
SIO_000300: 1.002367e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.7722e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.29e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1911
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GenotypeQuality
all individuals: 593
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5059
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6463
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1843
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.457814661134163e-5
allele num: 28920
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.03e-1

QD
type: SiteQuality
SIO_000300: 8.84e0

FS
type: SiteQuality
SIO_000300: 1.7722e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.028e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

DP
type: SiteQuality
SIO_000300: 1.002367e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5065
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 379
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1891
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.899644668299582e-5
allele num: 28987
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6842
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.135e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

FS
type: SiteQuality
SIO_000300: 1.2016e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: -2.725e0

MQ
type: SiteQuality
SIO_000300: 5.84e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.735e1

DP
type: SiteQuality
SIO_000300: 9.92205e5

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1771
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.587701359738815e-5
allele num: 27873
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.482359916987845e-4
allele num: 6746
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6151
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6185
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

FS
type: SiteQuality
SIO_000300: 4.022e0

DP
type: SiteQuality
SIO_000300: 9.57482e5

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1918
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1771
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6151
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.17540271947763e-5
allele num: 27873
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 1.293451899757478e-3
allele num: 6185
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6746
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.57482e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.308e1

FS
type: SiteQuality
SIO_000300: 4.022e0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 18500
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GenotypeQuality
all individuals: 1223
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 27881
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4891
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African
type: Population
allele count: 2
allele frequency: 3.245699448231094e-4
allele num: 6162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6741
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.87e-1

DP
type: SiteQuality
SIO_000300: 9.57551e5

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -8.1e-3

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1909
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GenotypeQuality
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GenotypeQuality
all individuals: 484
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 7.248477819657872e-5
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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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African
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 367
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MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1909
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GenotypeQuality
all individuals: 17526
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GenotypeQuality
all individuals: 389
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27289
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 357
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6054
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6039
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.331e0

QD
type: SiteQuality
SIO_000300: 1.005e1

DP
type: SiteQuality
SIO_000300: 9.40326e5

GenotypeQuality
all individuals: 1909
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 390
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 543
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 532
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.678363863753403e-5
allele num: 27186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6043
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6683
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4794
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.974e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

FS
type: SiteQuality
SIO_000300: 5.293e0

MQRankSum
type: SiteQuality
SIO_000300: -9.11e-1

DP
type: SiteQuality
SIO_000300: 9.36182e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.079e0

QD
type: SiteQuality
SIO_000300: 7.6e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.22e-1

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1395
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6681
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.689492325855962e-5
allele num: 27104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1677
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6011
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.671961210499916e-4
allele num: 5981
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.528e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.607e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

DP
type: SiteQuality
SIO_000300: 9.342e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

QD
type: SiteQuality
SIO_000300: 3.95e0

FS
type: SiteQuality
SIO_000300: 1.6838e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

GenotypeQuality
all individuals: 286
bin: 4.25e1
variant carriers: 31

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 28

GenotypeQuality
all individuals: 439
bin: 4.75e1
variant carriers: 55

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 34

GenotypeQuality
all individuals: 708
bin: 3.75e1
variant carriers: 35

GenotypeQuality
all individuals: 1318
bin: 6.75e1
variant carriers: 33

European (Non-Finnish)
type: Population
allele count: 493
allele frequency: 1.934623082054703e-2
allele num: 25483
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.004807692307692e-4
allele num: 6656
num of homozygotes: 0

African
type: Population
allele count: 254
allele frequency: 4.618181818181818e-2
allele num: 5500
num of homozygotes: 0

East Asian
type: Population
allele count: 15
allele frequency: 3.182686187141948e-3
allele num: 4713
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 56
allele frequency: 3.835616438356165e-2
allele num: 1460
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 2.388059701492537e-2
allele num: 335
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 8.450228156160216e-4
allele num: 5917
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.24e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.395e0

VQSLOD
type: SiteQuality
SIO_000300: -1.003e2

FS
type: SiteQuality
SIO_000300: 1.45641e2

DP
type: SiteQuality
SIO_000300: 9.6075e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.942e0

QD
type: SiteQuality
SIO_000300: 2.74e0

GenotypeQuality
all individuals: 26848
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 451
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1747
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.550147263990079e-4
allele num: 6451
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 341
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5264
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.957e1

MQ
type: SiteQuality
SIO_000300: 5.843e1

DP
type: SiteQuality
SIO_000300: 8.70971e5

VQSLOD
type: SiteQuality
SIO_000300: -4.125e-1

GenotypeQuality
all individuals: 365
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4249
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1701
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 339
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.964636542239686e-4
allele num: 5090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24657
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

DP
type: SiteQuality
SIO_000300: 8.45531e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.185e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

QD
type: SiteQuality
SIO_000300: 2.918e1

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1611
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4765
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: 0
allele frequency: 0.0e0
allele num: 23396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4039
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 7.92201e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.879e1

GenotypeQuality
all individuals: 493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6732
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5305
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.665049449524165e-5
allele num: 21436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4271
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6109
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

DP
type: SiteQuality
SIO_000300: 7.32119e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.53e1

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 226
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6448
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 301
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6103
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1434
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.893580761219466e-4
allele num: 5281
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4241
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3672
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21272
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.791e1

MQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.187e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.27388e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
all individuals: 486
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 2.41196333815726e-4
allele num: 4146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5236
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6073
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21073
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3621
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1421
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.86e-2

MQ
type: SiteQuality
SIO_000300: 5.875e1

QD
type: SiteQuality
SIO_000300: 1.441e1

MQRankSum
type: SiteQuality
SIO_000300: -1.002e0

FS
type: SiteQuality
SIO_000300: 3.979e0

DP
type: SiteQuality
SIO_000300: 7.23098e5

VQSLOD
type: SiteQuality
SIO_000300: -1.899e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 2315
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 875
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 472
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 258
bin: 9.25e1
variant carriers: 5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.663003663003663e-3
allele num: 273
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3288
num of homozygotes: 0

East Asian
type: Population
allele count: 115
allele frequency: 3.781650772772115e-2
allele num: 3041
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1207
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18067
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

DP
type: SiteQuality
SIO_000300: 6.62121e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.981e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

GenotypeQuality
all individuals: 627
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 663
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1852
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.143118427069044e-4
allele num: 8748
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47630
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

DP
type: SiteQuality
SIO_000300: 1.805973e6

QD
type: SiteQuality
SIO_000300: 2.695e1

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.218884120171674e-4
allele num: 9320
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9957
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47941
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

BaseQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.26e-1

ClippingRankSum
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SIO_000300: -1.004e0

QD
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SIO_000300: 1.269e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

DP
type: SiteQuality
SIO_000300: 1.857316e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084332075786314e-5
allele num: 47977
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10099
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.36e-1

MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: -9.673999999999999e0

FS
type: SiteQuality
SIO_000300: 2.779e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.861295e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47987
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174398120963006e-4
allele num: 8515
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.405e1

DP
type: SiteQuality
SIO_000300: 1.862069e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 2.963255630185698e-4
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47995
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.862599e6

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

BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.991e1

QD
type: SiteQuality
SIO_000300: 2.725e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.174398120963006e-4
allele num: 8515
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47998
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.45e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.86218e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.79e-1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506477854775535e-4
allele num: 6638
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47998
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.515e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.207e0

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

DP
type: SiteQuality
SIO_000300: 1.862063e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.166840285011876e-5
allele num: 47998
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 633
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Latino
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allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47997
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
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allele frequency: 1.506477854775535e-4
allele num: 6638
num of homozygotes: 0

MQRankSum
type: SiteQuality
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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East Asian
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allele frequency: 4.519433564326605e-4
allele num: 6638
num of homozygotes: 0

FS
type: SiteQuality
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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East Asian
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Other
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allele num: 633
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VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

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

European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 47996
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African
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allele frequency: 1.174398120963006e-4
allele num: 8515
num of homozygotes: 0

Latino
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allele num: 9321
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Other
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allele num: 633
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South Asian
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VQSLOD
type: SiteQuality
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MQ
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QD
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.167187565112306e-5
allele num: 47994
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10125
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.006e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.642e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.045e0

DP
type: SiteQuality
SIO_000300: 1.859997e6

QD
type: SiteQuality
SIO_000300: 2.478e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-1

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9603
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.103752759381898e-3
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.250520876739729e-5
allele num: 47996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10125
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.753e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

DP
type: SiteQuality
SIO_000300: 1.860103e6

QD
type: SiteQuality
SIO_000300: 2.242e1

FS
type: SiteQuality
SIO_000300: 5.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.554e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 670
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10125
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.893e0

DP
type: SiteQuality
SIO_000300: 1.854613e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.472e0

VQSLOD
type: SiteQuality
SIO_000300: -3.721e1

MQ
type: SiteQuality
SIO_000300: 5.527e1

FS
type: SiteQuality
SIO_000300: 5.4653e1

QD
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e0

GenotypeQuality
all individuals: 1644
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9612
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.174536058256989e-4
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.250390649415588e-5
allele num: 47997
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 6.622516556291391e-4
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10125
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.854206e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.26e-1