19-36940823-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940823
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940823
    reference: chr 19
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.316A>G
  hgvsp: ENSP00000394207.1:p.Met106Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.313A>G
  hgvsp: ENSP00000401259.2:p.Met105Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.313A>G
  hgvsp: ENSP00000411526.1:p.Met105Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.316A>G
  hgvsp: ENSP00000376010.2:p.Met106Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.1A>G
  hgvsp: ENSP00000465343.1:p.Met1?
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.316A>G
  hgvsp: ENSP00000400651.1:p.Met106Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.313A>G
  hgvsp: ENSP00000415520.2:p.Met105Val
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6977
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41097
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-36940825-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940825
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940825
    reference: chr 19
allele count: 8
allele frequency: 6.593696426216537e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.311T>A
  hgvsp: ENSP00000411526.1:p.Ile104Lys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.314T>A
  hgvsp: ENSP00000400651.1:p.Ile105Lys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.311T>A
  hgvsp: ENSP00000415520.2:p.Ile104Lys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-2T>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.311T>A
  hgvsp: ENSP00000401259.2:p.Ile104Lys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.314T>A
  hgvsp: ENSP00000394207.1:p.Ile105Lys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.314T>A
  hgvsp: ENSP00000376010.2:p.Ile105Lys
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41087
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile105Lys
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-36940846-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940846
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940846
    reference: chr 19
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.293T>C
  hgvsp: ENSP00000394207.1:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.293T>C
  hgvsp: ENSP00000376010.2:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.290T>C
  hgvsp: ENSP00000415520.2:p.Ile97Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.290T>C
  hgvsp: ENSP00000411526.1:p.Ile97Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.290T>C
  hgvsp: ENSP00000401259.2:p.Ile97Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.293T>C
  hgvsp: ENSP00000400651.1:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-23T>C
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile98Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

19-36940855-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940855
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940855
    reference: chr 19
allele count: 3
allele frequency: 2.48809859505366e-5
allele num: 120574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.284T>C
  hgvsp: ENSP00000400651.1:p.Ile95Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-32T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.284T>C
  hgvsp: ENSP00000376010.2:p.Ile95Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.281T>C
  hgvsp: ENSP00000415520.2:p.Ile94Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.281T>C
  hgvsp: ENSP00000401259.2:p.Ile94Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.281T>C
  hgvsp: ENSP00000411526.1:p.Ile94Thr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.284T>C
  hgvsp: ENSP00000394207.1:p.Ile95Thr
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40548
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile95Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

19-36940888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940888
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940888
    reference: chr 19
allele count: 1
allele frequency: 8.549346829902196e-6
allele num: 116968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.248G>A
  hgvsp: ENSP00000401259.2:p.Cys83Tyr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-65G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.248G>A
  hgvsp: ENSP00000411526.1:p.Cys83Tyr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.248G>A
  hgvsp: ENSP00000415520.2:p.Cys83Tyr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.251G>A
  hgvsp: ENSP00000400651.1:p.Cys84Tyr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.251G>A
  hgvsp: ENSP00000376010.2:p.Cys84Tyr
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.251G>A
  hgvsp: ENSP00000394207.1:p.Cys84Tyr
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6347
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37160
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys84Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

19-36940892-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940892
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940892
    reference: chr 19
allele count: 3
allele frequency: 2.577673907066263e-5
allele num: 116384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.244A>G
  hgvsp: ENSP00000415520.2:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-69A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.247A>G
  hgvsp: ENSP00000400651.1:p.Arg83Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.247A>G
  hgvsp: ENSP00000394207.1:p.Arg83Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.244A>G
  hgvsp: ENSP00000411526.1:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.247A>G
  hgvsp: ENSP00000376010.2:p.Arg83Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.244A>G
  hgvsp: ENSP00000401259.2:p.Arg82Gly
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg83Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-36940893-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940893
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940893
    reference: chr 19
allele count: 1
allele frequency: 8.607629803057431e-6
allele num: 116176
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.246A>C
  hgvsp: ENST00000454319.1:c.246A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.243A>C
  hgvsp: ENST00000424129.2:c.243A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-70A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.243A>C
  hgvsp: ENST00000452939.1:c.243A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.246A>C
  hgvsp: ENST00000427002.1:c.246A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.246A>C
  hgvsp: ENST00000392170.2:c.246A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.243A>C
  hgvsp: ENST00000434377.2:c.243A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4428
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser82Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-36940910-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940910
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940910
    reference: chr 19
allele count: 1
allele frequency: 8.921720821512054e-6
allele num: 112086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-7C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-7C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-7C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-7C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-7C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-7C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-7C>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13843
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
hgvs: c.236-7C>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-36940912-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940912
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940912
    reference: chr 19
allele count: 1
allele frequency: 8.913291500285225e-6
allele num: 112192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-9T>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5809
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4413
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

19-36940924-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940924
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940924
    reference: chr 19
allele count: 1
allele frequency: 9.191852342083978e-6
allele num: 108792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-21T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-21T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-21T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-21T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-21T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-21T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-21T>C
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7742
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4409
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-36940928-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940928
    reference: chr 19
allele count: 1
allele frequency: 9.270761871210575e-6
allele num: 107866
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-25T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-25T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-25T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-25T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-25T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-25T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-25T>C
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7910
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26934
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

19-36940933-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940933
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940933
    reference: chr 19
allele count: 13
allele frequency: 1.218392097321412e-4
allele num: 106698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-30G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-30G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-30G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-30G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-30G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-30G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-30G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15274
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11310
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 4630
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

19-36940934-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940934
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940934
    reference: chr 19
allele count: 1
allele frequency: 9.391787820729554e-6
allele num: 106476
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-31T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-31T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-31T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-31T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-31T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-31T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-31T>C
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4565
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8062
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-36940940-C-CTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940943
    reference: chr 19
allele count: 12
allele frequency: 1.143728555089592e-4
allele num: 104920
alternate allele: CTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-38_-80-37insAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-38_233-37insAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-38_236-37insAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-38_233-37insAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-38_236-37insAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-38_233-37insAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-38_236-37insAAA
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7470
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4414
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 18422
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

19-36940940-C-CTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940944
    reference: chr 19
allele count: 8
allele frequency: 7.624857033930614e-5
allele num: 104920
alternate allele: CTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-38_-80-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-38_236-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-38_233-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-38_233-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-38_233-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-38_236-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-38_236-37insAAAA
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

19-36940940-C-CTTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940945
    reference: chr 19
allele count: 15
allele frequency: 1.42966069386199e-4
allele num: 104920
alternate allele: CTTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-38_233-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-38_236-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-38_236-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-38_236-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-38_233-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-38_233-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-38_-80-37insAAAAA
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7470
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

19-36940940-C-CTTTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940946
    reference: chr 19
allele count: 4
allele frequency: 3.812428516965307e-5
allele num: 104920
alternate allele: CTTTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-38_236-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-38_233-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-38_233-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-38_236-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-38_236-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-38_-80-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-38_233-37insAAAAAA
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4414
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

19-36940940-C-CTTTTTTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940949
    reference: chr 19
allele count: 4
allele frequency: 3.812428516965307e-5
allele num: 104920
alternate allele: CTTTTTTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7470
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4414
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

19-36940940-C-CTTTTTTTTTTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940953
    reference: chr 19
allele count: 1
allele frequency: 9.531071292413268e-6
allele num: 104920
alternate allele: CTTTTTTTTTTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7470
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-36940943-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940943
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940943
    reference: chr 19
allele count: 67
allele frequency: 6.441936042151414e-4
allele num: 104006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-40C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-40C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-40C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-40C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-40C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-40C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-40C>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10692
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10111
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4528
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4487
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 2
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-36940944-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36940944
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36940944
    reference: chr 19
allele count: 7
allele frequency: 6.726112691213775e-5
allele num: 104072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.233-41A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.233-41A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.236-41A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.236-41A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.233-41A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-80-41A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.236-41A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2579
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15272
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4392
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3709
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36963771-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963771
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963771
    reference: chr 19
allele count: 2
allele frequency: 1.682595234890295e-5
allele num: 118864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.232+42A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.235+42A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.235+42A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.232+42A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.232+42A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3680A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3680A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.235+42A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

19-36963772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963772
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963772
    reference: chr 19
allele count: 1
allele frequency: 8.422613031466883e-6
allele num: 118728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.232+41G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.235+41G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.235+41G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3679G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.232+41G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.232+41G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.235+41G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3679G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

19-36963788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963788
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963788
    reference: chr 19
allele count: 10
allele frequency: 8.379279717115516e-5
allele num: 119342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.232+25C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.232+25C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3663C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.235+25C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.235+25C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.232+25C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3663C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.235+25C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

19-36963797-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963797
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963797
    reference: chr 19
allele count: 1
allele frequency: 8.345434212942099e-6
allele num: 119826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.235+16C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.232+16C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.235+16C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.235+16C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3654C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.232+16C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3654C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.232+16C>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39359
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

19-36963810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963810
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963810
    reference: chr 19
allele count: 4
allele frequency: 3.318951211417192e-5
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.232+3A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.235+3A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.235+3A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.235+3A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3641A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.232+3A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3641A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.232+3A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 8.25e1
  variant carriers: 0
hgvs: c.235+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-36963824-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963824
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963824
    reference: chr 19
allele count: 1
allele frequency: 8.262823902696986e-6
allele num: 121024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.221G>A
  hgvsp: ENSP00000411526.1:p.Gly74Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.221G>A
  hgvsp: ENSP00000401259.2:p.Gly74Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.224G>A
  hgvsp: ENSP00000394207.1:p.Gly75Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.224G>A
  hgvsp: ENSP00000376010.2:p.Gly75Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.221G>A
  hgvsp: ENSP00000415520.2:p.Gly74Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.224G>A
  hgvsp: ENSP00000400651.1:p.Gly75Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3627G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3627G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly75Asp
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

19-36963830-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963830
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963830
    reference: chr 19
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.218C>G
  hgvsp: ENSP00000376010.2:p.Thr73Arg
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.218C>G
  hgvsp: ENSP00000394207.1:p.Thr73Arg
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.218C>G
  hgvsp: ENSP00000400651.1:p.Thr73Arg
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.215C>G
  hgvsp: ENSP00000415520.2:p.Thr72Arg
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.215C>G
  hgvsp: ENSP00000411526.1:p.Thr72Arg
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.215C>G
  hgvsp: ENSP00000401259.2:p.Thr72Arg
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3621C>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3621C>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9993
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  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: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2656
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr73Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

19-36963831-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963831
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963831
    reference: chr 19
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.217A>C
  hgvsp: ENSP00000400651.1:p.Thr73Pro
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3620A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.217A>C
  hgvsp: ENSP00000376010.2:p.Thr73Pro
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.214A>C
  hgvsp: ENSP00000401259.2:p.Thr72Pro
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.214A>C
  hgvsp: ENSP00000415520.2:p.Thr72Pro
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3620A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.217A>C
  hgvsp: ENSP00000394207.1:p.Thr73Pro
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.214A>C
  hgvsp: ENSP00000411526.1:p.Thr72Pro
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2660
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr73Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

19-36963841-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963841
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963841
    reference: chr 19
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.207C>G
  hgvsp: ENSP00000394207.1:p.Asp69Glu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.207C>G
  hgvsp: ENSP00000376010.2:p.Asp69Glu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.204C>G
  hgvsp: ENSP00000415520.2:p.Asp68Glu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3610C>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.204C>G
  hgvsp: ENSP00000401259.2:p.Asp68Glu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.204C>G
  hgvsp: ENSP00000411526.1:p.Asp68Glu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3610C>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.207C>G
  hgvsp: ENSP00000400651.1:p.Asp69Glu
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10090
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp69Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

19-36963849-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963849
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963849
    reference: chr 19
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.199T>C
  hgvsp: ENST00000427002.1:c.199T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3602T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.199T>C
  hgvsp: ENST00000392170.2:c.199T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.196T>C
  hgvsp: ENST00000434377.2:c.196T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3602T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.196T>C
  hgvsp: ENST00000424129.2:c.196T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.196T>C
  hgvsp: ENST00000452939.1:c.196T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.199T>C
  hgvsp: ENST00000454319.1:c.199T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu67Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

19-36963850-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963850
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963850
    reference: chr 19
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.198G>C
  hgvsp: ENSP00000400651.1:p.Trp66Cys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.195G>C
  hgvsp: ENSP00000401259.2:p.Trp65Cys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.195G>C
  hgvsp: ENSP00000411526.1:p.Trp65Cys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3601G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.198G>C
  hgvsp: ENSP00000394207.1:p.Trp66Cys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3601G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.198G>C
  hgvsp: ENSP00000376010.2:p.Trp66Cys
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.195G>C
  hgvsp: ENSP00000415520.2:p.Trp65Cys
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39355
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp66Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-36963856-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963856
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963856
    reference: chr 19
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.189G>T
  hgvsp: ENSP00000415520.2:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.189G>T
  hgvsp: ENSP00000401259.2:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.189G>T
  hgvsp: ENSP00000411526.1:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.192G>T
  hgvsp: ENSP00000394207.1:p.Glu64Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.192G>T
  hgvsp: ENSP00000376010.2:p.Glu64Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3595G>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.192G>T
  hgvsp: ENSP00000400651.1:p.Glu64Asp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3595G>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu64Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum

19-36963856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963856
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963856
    reference: chr 19
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.192G>A
  hgvsp: ENST00000454319.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.192G>A
  hgvsp: ENST00000427002.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.192G>A
  hgvsp: ENST00000392170.2:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3595G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.189G>A
  hgvsp: ENST00000434377.2:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.189G>A
  hgvsp: ENST00000424129.2:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.189G>A
  hgvsp: ENST00000452939.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3595G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu64Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/19-36963872-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963872
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963872
    reference: chr 19
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.173T>G
  hgvsp: ENSP00000401259.2:p.Leu58Trp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3579T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.176T>G
  hgvsp: ENSP00000376010.2:p.Leu59Trp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.176T>G
  hgvsp: ENSP00000394207.1:p.Leu59Trp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.173T>G
  hgvsp: ENSP00000411526.1:p.Leu58Trp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.173T>G
  hgvsp: ENSP00000415520.2:p.Leu58Trp
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3579T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.176T>G
  hgvsp: ENSP00000400651.1:p.Leu59Trp
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu59Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-36963877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963877
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963877
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3574C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.168C>T
  hgvsp: ENST00000452939.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.171C>T
  hgvsp: ENST00000427002.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.168C>T
  hgvsp: ENST00000434377.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.171C>T
  hgvsp: ENST00000454319.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3574C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.168C>T
  hgvsp: ENST00000424129.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.171C>T
  hgvsp: ENST00000392170.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1872
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser57Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

19-36963890-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963890
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963890
    reference: chr 19
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.155C>T
  hgvsp: ENSP00000411526.1:p.Pro52Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.158C>T
  hgvsp: ENSP00000400651.1:p.Pro53Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.155C>T
  hgvsp: ENSP00000415520.2:p.Pro52Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.155C>T
  hgvsp: ENSP00000401259.2:p.Pro52Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.158C>T
  hgvsp: ENSP00000376010.2:p.Pro53Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3561C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.158C>T
  hgvsp: ENSP00000394207.1:p.Pro53Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3561C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro53Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-36963900-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963900
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963900
    reference: chr 19
allele count: 4
allele frequency: 3.311861431717697e-5
allele num: 120778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3551A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3551A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.148A>G
  hgvsp: ENSP00000376010.2:p.Ile50Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.145A>G
  hgvsp: ENSP00000415520.2:p.Ile49Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.148A>G
  hgvsp: ENSP00000400651.1:p.Ile50Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.145A>G
  hgvsp: ENSP00000401259.2:p.Ile49Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.148A>G
  hgvsp: ENSP00000394207.1:p.Ile50Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.145A>G
  hgvsp: ENSP00000411526.1:p.Ile49Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.563A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39351
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile50Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-36963907-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963907
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963907
    reference: chr 19
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.141G>C
  hgvsp: ENST00000454319.1:c.141G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.556G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.141G>C
  hgvsp: ENST00000392170.2:c.141G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3544G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.138G>C
  hgvsp: ENST00000424129.2:c.138G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.141G>C
  hgvsp: ENST00000427002.1:c.141G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.138G>C
  hgvsp: ENST00000452939.1:c.138G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3544G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.138G>C
  hgvsp: ENST00000434377.2:c.138G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 6.75e1
  variant carriers: 0
hgvs: c.138G>C
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

19-36963910-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963910
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963910
    reference: chr 19
allele count: 7
allele frequency: 5.817335660267598e-5
allele num: 120330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3541A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.138A>T
  hgvsp: ENST00000427002.1:c.138A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.138A>T
  hgvsp: ENST00000454319.1:c.138A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3541A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-2A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.553A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-2A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.138A>T
  hgvsp: ENST00000392170.2:c.138A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-2A>T
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8684
  bin: 6.25e1
  variant carriers: 0
hgvs: c.137-2A>T
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-36963917-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963917
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963917
    reference: chr 19
allele count: 1
allele frequency: 8.340144451301897e-6
allele num: 119902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-6T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.546T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-6T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-6T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-9T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3534T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3534T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-9T>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
hgvs: c.137-6T>G
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

19-36963928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963928
    reference: chr 19
allele count: 2
allele frequency: 1.67470525187567e-5
allele num: 119424
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-17G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3523G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-20G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.535G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3523G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-17G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-20G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-17G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-20G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6367
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39337
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

19-36963937-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963937
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963937
    reference: chr 19
allele count: 1
allele frequency: 8.396728634523989e-6
allele num: 119094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3514A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-26A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-26A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-29A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-29A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3514A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-26A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.526A>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-29A>C
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum

19-36963944-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963944
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963944
    reference: chr 19
allele count: 1
allele frequency: 8.434263351438885e-6
allele num: 118564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-33A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3507A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-36A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-36A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-33A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.519A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3507A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-36A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-33A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39296
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-36963955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963955
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963955
    reference: chr 19
allele count: 3
allele frequency: 2.552756977535739e-5
allele num: 117520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-44A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-44A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-47A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-44A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.508A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3496A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-47A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-47A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3496A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-36963956-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963956
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963956
    reference: chr 19
allele count: 2
allele frequency: 1.702156632453318e-5
allele num: 117498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-45T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-45T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-48T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-48T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-48T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3495T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-45T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.507T>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3495T>G
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2939
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

19-36963957-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36963957
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36963957
    reference: chr 19
allele count: 1
allele frequency: 8.518032675173342e-6
allele num: 117398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.137-49C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.137-46C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.137-49C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.137-46C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3494C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.506C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.137-49C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.137-46C>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3494C>A
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-36964195-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964195
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964195
    reference: chr 19
allele count: 3
allele frequency: 2.477823479855295e-5
allele num: 121074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3256T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.322T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.136+39T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.136+39T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.136+39T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.136+39T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3256T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.268T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.136+39T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.136+39T>C
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

19-36964225-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964225
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964225
    reference: chr 19
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3226A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3226A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.238A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.136+9A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.136+9A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.136+9A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.136+9A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.136+9A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.292A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.136+9A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

19-36964226-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964226
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964226
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.136+8C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3225C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.136+8C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.136+8C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.291C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.237C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.136+8C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.136+8C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3225C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.136+8C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 7.75e1
  variant carriers: 0
hgvs: c.136+8C>T
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

19-36964237-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964237
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964237
    reference: chr 19
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.133A>G
  hgvsp: ENSP00000394207.1:p.Met45Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.133A>G
  hgvsp: ENSP00000376010.2:p.Met45Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.226A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.133A>G
  hgvsp: ENSP00000401259.2:p.Met45Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3214A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.133A>G
  hgvsp: ENSP00000411526.1:p.Met45Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.133A>G
  hgvsp: ENSP00000400651.1:p.Met45Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3214A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.133A>G
  hgvsp: ENSP00000415520.2:p.Met45Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.280A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met45Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

19-36964243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964243
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964243
    reference: chr 19
allele count: 4
allele frequency: 3.30016665841625e-5
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3208G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.127G>A
  hgvsp: ENSP00000400651.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.127G>A
  hgvsp: ENSP00000415520.2:p.Val43Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.127G>A
  hgvsp: ENSP00000376010.2:p.Val43Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3208G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.220G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.127G>A
  hgvsp: ENSP00000411526.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.274G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.127G>A
  hgvsp: ENSP00000401259.2:p.Val43Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.127G>A
  hgvsp: ENSP00000394207.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val43Ile
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

19-36964248-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964248
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964248
    reference: chr 19
allele count: 2
allele frequency: 1.650028875505322e-5
allele num: 121210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3203A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.122A>G
  hgvsp: ENSP00000415520.2:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.122A>G
  hgvsp: ENSP00000376010.2:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3203A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.122A>G
  hgvsp: ENSP00000401259.2:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.122A>G
  hgvsp: ENSP00000411526.1:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.215A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.122A>G
  hgvsp: ENSP00000394207.1:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.269A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.122A>G
  hgvsp: ENSP00000400651.1:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn41Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

19-36964267-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964267
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964267
    reference: chr 19
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3184A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.103A>G
  hgvsp: ENSP00000415520.2:p.Met35Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.103A>G
  hgvsp: ENSP00000411526.1:p.Met35Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3184A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.103A>G
  hgvsp: ENSP00000400651.1:p.Met35Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.103A>G
  hgvsp: ENSP00000376010.2:p.Met35Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.103A>G
  hgvsp: ENSP00000401259.2:p.Met35Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.103A>G
  hgvsp: ENSP00000394207.1:p.Met35Val
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.196A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.250A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met35Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

19-36964280-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964280
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964280
    reference: chr 19
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.237A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.90A>T
  hgvsp: ENSP00000394207.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.90A>T
  hgvsp: ENSP00000400651.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3171A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.90A>T
  hgvsp: ENSP00000401259.2:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.90A>T
  hgvsp: ENSP00000415520.2:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3171A>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.90A>T
  hgvsp: ENSP00000376010.2:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.90A>T
  hgvsp: ENSP00000411526.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.183A>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu30Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

19-36964285-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964285
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964285
    reference: chr 19
allele count: 2
allele frequency: 1.656397005234214e-5
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.85G>A
  hgvsp: ENSP00000400651.1:p.Asp29Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.178G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.85G>A
  hgvsp: ENSP00000401259.2:p.Asp29Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3166G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.85G>A
  hgvsp: ENSP00000376010.2:p.Asp29Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.85G>A
  hgvsp: ENSP00000411526.1:p.Asp29Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.232G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.85G>A
  hgvsp: ENSP00000394207.1:p.Asp29Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.85G>A
  hgvsp: ENSP00000415520.2:p.Asp29Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3166G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp29Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

19-36964296-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964296
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964296
    reference: chr 19
allele count: 1
allele frequency: 8.301235223801302e-6
allele num: 120464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3155A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.74A>G
  hgvsp: ENSP00000401259.2:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3155A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.74A>G
  hgvsp: ENSP00000376010.2:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.74A>G
  hgvsp: ENSP00000394207.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.74A>G
  hgvsp: ENSP00000411526.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.221A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.74A>G
  hgvsp: ENSP00000415520.2:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.74A>G
  hgvsp: ENSP00000400651.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.167A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp25Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

19-36964316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964316
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964316
    reference: chr 19
allele count: 1
allele frequency: 8.346688034188035e-6
allele num: 119808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.54G>A
  hgvsp: ENST00000452939.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.201G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.54G>A
  hgvsp: ENST00000427002.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3135G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.54G>A
  hgvsp: ENST00000434377.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.54G>A
  hgvsp: ENST00000392170.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.54G>A
  hgvsp: ENST00000424129.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.54G>A
  hgvsp: ENST00000454319.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.147G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3135G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu18Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS

19-36964319-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964319
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964319
    reference: chr 19
allele count: 1
allele frequency: 8.356313194618534e-6
allele num: 119670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.144G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.51G>C
  hgvsp: ENSP00000411526.1:p.Gln17His
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.51G>C
  hgvsp: ENSP00000376010.2:p.Gln17His
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.51G>C
  hgvsp: ENSP00000394207.1:p.Gln17His
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.51G>C
  hgvsp: ENSP00000401259.2:p.Gln17His
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.51G>C
  hgvsp: ENSP00000400651.1:p.Gln17His
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.198G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3132G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3132G>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.51G>C
  hgvsp: ENSP00000415520.2:p.Gln17His
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln17His
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

19-36964325-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964325
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964325
    reference: chr 19
allele count: 11
allele frequency: 9.222771862161482e-5
allele num: 119270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.45C>T
  hgvsp: ENST00000424129.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3126C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.45C>T
  hgvsp: ENST00000434377.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.45C>T
  hgvsp: ENST00000392170.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3126C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.45C>T
  hgvsp: ENST00000427002.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.45C>T
  hgvsp: ENST00000454319.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.45C>T
  hgvsp: ENST00000452939.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.192C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.138C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35176
  bin: 9.75e1
  variant carriers: 11
hgvs: p.Phe15Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-36964333-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964333
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964333
    reference: chr 19
allele count: 9
allele frequency: 7.569386038687972e-5
allele num: 118900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.130G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.37G>A
  hgvsp: ENSP00000411526.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.37G>A
  hgvsp: ENSP00000376010.2:p.Val13Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.37G>A
  hgvsp: ENSP00000415520.2:p.Val13Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.37G>A
  hgvsp: ENSP00000401259.2:p.Val13Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3118G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3118G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.37G>A
  hgvsp: ENSP00000400651.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.184G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.37G>A
  hgvsp: ENSP00000394207.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val13Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

19-36964334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964334
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964334
    reference: chr 19
allele count: 8
allele frequency: 6.729022273063724e-5
allele num: 118888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.36C>T
  hgvsp: ENST00000392170.2:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.36C>T
  hgvsp: ENST00000452939.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.36C>T
  hgvsp: ENST00000454319.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.129C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.36C>T
  hgvsp: ENST00000424129.2:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.183C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.36C>T
  hgvsp: ENST00000427002.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.36C>T
  hgvsp: ENST00000434377.2:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3117C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3117C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser12Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-36964334-G-GGACA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964334
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964338
    reference: chr 19
allele count: 1
allele frequency: 8.411277841329655e-6
allele num: 118888
alternate allele: GGACA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.32_35dupTGTC
  hgvsp: ENSP00000376010.2:p.Asp14ArgfsTer13
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.32_35dupTGTC
  hgvsp: ENSP00000400651.1:p.Asp14ArgfsTer13
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.179_182dupTGTC
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.32_35dupTGTC
  hgvsp: ENSP00000411526.1:p.Asp14ArgfsTer13
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.32_35dupTGTC
  hgvsp: ENSP00000394207.1:p.Asp14ArgfsTer13
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3113_497+3116dupTGTC
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.32_35dupTGTC
  hgvsp: ENSP00000401259.2:p.Asp14ArgfsTer13
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.125_128dupTGTC
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.32_35dupTGTC
  hgvsp: ENSP00000415520.2:p.Asp14ArgfsTer13
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3113_-81+3116dupTGTC
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp14ArgfsTer13
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

19-36964344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964344
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964344
    reference: chr 19
allele count: 2
allele frequency: 1.692792091275349e-5
allele num: 118148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.26G>A
  hgvsp: ENSP00000411526.1:p.Ser9Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.26G>A
  hgvsp: ENSP00000376010.2:p.Ser9Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.26G>A
  hgvsp: ENSP00000394207.1:p.Ser9Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.26G>A
  hgvsp: ENSP00000401259.2:p.Ser9Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3107G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.173G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3107G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.26G>A
  hgvsp: ENSP00000415520.2:p.Ser9Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.26G>A
  hgvsp: ENSP00000400651.1:p.Ser9Asn
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.119G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser9Asn
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-36964355-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964355
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964355
    reference: chr 19
allele count: 1
allele frequency: 8.499932000543996e-6
allele num: 117648
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.15A>G
  hgvsp: ENST00000427002.1:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3096A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.162A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.15A>G
  hgvsp: ENST00000434377.2:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.15A>G
  hgvsp: ENST00000424129.2:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.15A>G
  hgvsp: ENST00000392170.2:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.15A>G
  hgvsp: ENST00000452939.1:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3096A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.108A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.15A>G
  hgvsp: ENST00000454319.1:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35164
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser5Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

19-36964356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964356
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964356
    reference: chr 19
allele count: 1
allele frequency: 8.504413790757403e-6
allele num: 117586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.14C>T
  hgvsp: ENSP00000400651.1:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.14C>T
  hgvsp: ENSP00000394207.1:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.14C>T
  hgvsp: ENSP00000415520.2:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.14C>T
  hgvsp: ENSP00000401259.2:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.161C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3095C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3095C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.14C>T
  hgvsp: ENSP00000376010.2:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.14C>T
  hgvsp: ENSP00000411526.1:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.107C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser5Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-36964359-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964359
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964359
    reference: chr 19
allele count: 1
allele frequency: 8.518032675173342e-6
allele num: 117398
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.11A>G
  hgvsp: ENSP00000394207.1:p.Glu4Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.11A>G
  hgvsp: ENSP00000411526.1:p.Glu4Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.11A>G
  hgvsp: ENSP00000376010.2:p.Glu4Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.11A>G
  hgvsp: ENSP00000401259.2:p.Glu4Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.104A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.11A>G
  hgvsp: ENSP00000415520.2:p.Glu4Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.11A>G
  hgvsp: ENSP00000400651.1:p.Glu4Gly
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.158A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3092A>G
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3092A>G
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu4Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

19-36964376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964376
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964376
    reference: chr 19
allele count: 28364
allele frequency: 2.447197680839315e-1
allele num: 115904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.10-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.10-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3075G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.157-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.10-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.10-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.10-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3075G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.10-16G>A
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.103-16G>A
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 3.75e1
  variant carriers: 302
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 7.5e0
  variant carriers: 719
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 4.75e1
  variant carriers: 863
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 2.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 1.25e1
  variant carriers: 1137
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 7.25e1
  variant carriers: 2019
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 6.75e1
  variant carriers: 2084
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 8.75e1
  variant carriers: 1431
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 7.75e1
  variant carriers: 1848
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 2.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.25e1
  variant carriers: 1659
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 6.25e1
  variant carriers: 1895
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 9.25e1
  variant carriers: 1169
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 4.25e1
  variant carriers: 547
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 3.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 5.25e1
  variant carriers: 1305
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 5.75e1
  variant carriers: 1635
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 9.75e1
  variant carriers: 5990
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 7.25e1
  variant carriers: 78
genotype quality: GenotypeQuality
  all individuals: 4896
  bin: 6.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 74
num of homozygotes: 3662
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

19-36964377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964377
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964377
    reference: chr 19
allele count: 2
allele frequency: 1.751098814506103e-5
allele num: 114214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3074C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.10-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.10-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.10-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3074C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.157-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.10-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.10-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.10-17C>T
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.103-17C>T
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-36964379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36964379
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36964379
    reference: chr 19
allele count: 4
allele frequency: 3.521312745391482e-5
allele num: 113594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000376010
  ensembl transcript: ENST00000392170
  gene symbol: ZNF566
  hgvsc: ENST00000392170.2:c.10-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000480361
  gene symbol: ZNF566
  hgvsc: ENST00000480361.1:n.157-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000465343
  ensembl transcript: ENST00000493391
  gene symbol: ZNF566
  hgvsc: ENST00000493391.1:c.-81+3072T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000401259
  ensembl transcript: ENST00000424129
  gene symbol: ZNF566
  hgvsc: ENST00000424129.2:c.10-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000411526
  ensembl transcript: ENST00000452939
  gene symbol: ZNF566
  hgvsc: ENST00000452939.1:c.10-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000460937
  gene symbol: ZNF566
  hgvsc: ENST00000460937.1:n.103-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000400651
  ensembl transcript: ENST00000427002
  gene symbol: ZNF566
  hgvsc: ENST00000427002.1:c.10-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl transcript: ENST00000472909
  gene symbol: ZNF566
  hgvsc: ENST00000472909.2:n.497+3072T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000415520
  ensembl transcript: ENST00000434377
  gene symbol: ZNF566
  hgvsc: ENST00000434377.2:c.10-19T>C
  variant of: http://identifiers.org/hgnc/25919
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186017
  ensembl protein: ENSP00000394207
  ensembl transcript: ENST00000454319
  gene symbol: ZNF566
  hgvsc: ENST00000454319.1:c.10-19T>C
  variant of: http://identifiers.org/hgnc/25919
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22821
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3871
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1700
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4460
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 1.202e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.27e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.23e0

DP
type: SiteQuality
SIO_000300: 1.791165e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6971
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1029
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4459
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.84613520717228e-4
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 2.193e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.7905e6

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

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

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4446
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1025
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.779705e6

VQSLOD
type: SiteQuality
SIO_000300: -4.54e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.93e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.703e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.807e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6805
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4444
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1684
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.522703973949225e-5
allele num: 66332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.351e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

DP
type: SiteQuality
SIO_000300: 1.774371e6

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.452e1

GenotypeQuality
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4434
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164686699277894e-4
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14640
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

FS
type: SiteQuality
SIO_000300: 8.227e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 1.70728e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e0

QD
type: SiteQuality
SIO_000300: 1.325e1

VQSLOD
type: SiteQuality
SIO_000300: 3.94e-1

GenotypeQuality
all individuals: 4431
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64790
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.508771929824561e-4
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14362
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.73e-1

DP
type: SiteQuality
SIO_000300: 1.696767e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

QD
type: SiteQuality
SIO_000300: 1.5e1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 2.165e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.06e0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14278
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545451735542299e-5
allele num: 64706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: -2.308e-1

QD
type: SiteQuality
SIO_000300: 1.665e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.18e-1

DP
type: SiteQuality
SIO_000300: 1.693012e6

GenotypeQuality
all individuals: 2334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6445
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4413
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.95924864692773e-5
allele num: 12564
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.647e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.622693e6

VQSLOD
type: SiteQuality
SIO_000300: -6.231e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.279e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

GenotypeQuality
all individuals: 2331
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584987003106575e-5
allele num: 63092
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

QD
type: SiteQuality
SIO_000300: 1.727e1

VQSLOD
type: SiteQuality
SIO_000300: -8.405e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

DP
type: SiteQuality
SIO_000300: 1.621541e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.083e0

MQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

GenotypeQuality
all individuals: 341
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.097694840834248e-4
allele num: 9110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

DP
type: SiteQuality
SIO_000300: 1.534087e6

QD
type: SiteQuality
SIO_000300: 1.858e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.251e0

VQSLOD
type: SiteQuality
SIO_000300: -6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e0

MQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

GenotypeQuality
all individuals: 272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1257
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5063
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.952551477170994e-5
allele num: 11170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.311e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 1.507978e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 8.073e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 6.82e0

GenotypeQuality
all individuals: 2443
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.147553441041398e-4
allele num: 60534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8940
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.457485e6

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 6.043e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.022e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

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

GenotypeQuality
all individuals: 161
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
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variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 679
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.654916757687088e-5
allele num: 60426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

MQ
type: SiteQuality
SIO_000300: 5.906e1

QD
type: SiteQuality
SIO_000300: 1.477e1

VQSLOD
type: SiteQuality
SIO_000300: -1.394e0

FS
type: SiteQuality
SIO_000300: 3.245e0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

DP
type: SiteQuality
SIO_000300: 1.445724e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

GenotypeQuality
all individuals: 1547
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1574
bin: 4.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.814552712756306e-4
allele num: 11022
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.135073779795687e-3
allele num: 8810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.826e0

DP
type: SiteQuality
SIO_000300: 1.387577e6

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

FS
type: SiteQuality
SIO_000300: 6.897e0

QD
type: SiteQuality
SIO_000300: 2.6e0

VQSLOD
type: SiteQuality
SIO_000300: -5.411e-1

GenotypeQuality
all individuals: 1524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18422
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 9.080590238365494e-4
allele num: 8810
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

FS
type: SiteQuality
SIO_000300: 6.897e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

DP
type: SiteQuality
SIO_000300: 1.387577e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.826e0

VQSLOD
type: SiteQuality
SIO_000300: -5.411e-1

QD
type: SiteQuality
SIO_000300: 2.6e0

GenotypeQuality
all individuals: 2382
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18422
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 1.70261066969353e-3
allele num: 8810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.826e0

FS
type: SiteQuality
SIO_000300: 6.897e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 2.6e0

DP
type: SiteQuality
SIO_000300: 1.387577e6

VQSLOD
type: SiteQuality
SIO_000300: -5.411e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 772
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variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.540295119182747e-4
allele num: 8810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

MQ
type: SiteQuality
SIO_000300: 5.705e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -5.411e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.826e0

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

FS
type: SiteQuality
SIO_000300: 6.897e0

QD
type: SiteQuality
SIO_000300: 2.6e0

DP
type: SiteQuality
SIO_000300: 1.387577e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

GenotypeQuality
all individuals: 1524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2832
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2092
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GenotypeQuality
all individuals: 3843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18422
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.540295119182747e-4
allele num: 8810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.411e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.826e0

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 6.897e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

QD
type: SiteQuality
SIO_000300: 2.6e0

DP
type: SiteQuality
SIO_000300: 1.387577e6

MQ
type: SiteQuality
SIO_000300: 5.705e1

GenotypeQuality
all individuals: 3843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
all individuals: 1574
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18422
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.135073779795687e-4
allele num: 8810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.705e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

QD
type: SiteQuality
SIO_000300: 2.6e0

FS
type: SiteQuality
SIO_000300: 6.897e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.826e0

VQSLOD
type: SiteQuality
SIO_000300: -5.411e-1

DP
type: SiteQuality
SIO_000300: 1.387577e6

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

GenotypeQuality
all individuals: 1095
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2281
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 985
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2001
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2053
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4419
bin: 9.75e1
variant carriers: 38

GenotypeQuality
all individuals: 1509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16054
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 674
bin: 8.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

African
type: Population
allele count: 65
allele frequency: 7.565176908752328e-3
allele num: 8592
num of homozygotes: 2

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

Latino
type: Population
allele count: 2
allele frequency: 1.824817518248175e-4
allele num: 10960
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59248
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.851e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e0

QD
type: SiteQuality
SIO_000300: 4.35e0

VQSLOD
type: SiteQuality
SIO_000300: -4.654e0

FS
type: SiteQuality
SIO_000300: 4.556e0

DP
type: SiteQuality
SIO_000300: 1.364795e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.358e0

MQ
type: SiteQuality
SIO_000300: 5.777e1

GenotypeQuality
all individuals: 305
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4628
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variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7009
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variant carriers: 1

GenotypeQuality
all individuals: 2133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2923
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1506
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 6.008411776487082e-4
allele num: 9986
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8754
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.298701298701299e-3
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59204
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.357398e6

VQSLOD
type: SiteQuality
SIO_000300: 6.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.071e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 1.736e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

GenotypeQuality
all individuals: 587
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39359
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.034901365705614e-5
allele num: 65900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.5e0

DP
type: SiteQuality
SIO_000300: 3.337925e6

VQSLOD
type: SiteQuality
SIO_000300: -8.06e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

QD
type: SiteQuality
SIO_000300: 1.65e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 7.21e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517911353976928e-5
allele num: 65880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.35e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

FS
type: SiteQuality
SIO_000300: 2.946e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.092e1

DP
type: SiteQuality
SIO_000300: 3.338221e6

VQSLOD
type: SiteQuality
SIO_000300: 8.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.19e-1

GenotypeQuality
all individuals: 2496
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 39360
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 659
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7127
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.970572779821335e-4
allele num: 15224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.571856922191598e-5
allele num: 66034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 3.353778e6

FS
type: SiteQuality
SIO_000300: 1.303e0

QD
type: SiteQuality
SIO_000300: 1.327e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 895
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
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variant carriers: 0

GenotypeQuality
all individuals: 1880
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 8102
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variant carriers: 0

GenotypeQuality
all individuals: 440
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variant carriers: 0

GenotypeQuality
all individuals: 2004
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variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.38e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.31e-1

DP
type: SiteQuality
SIO_000300: 3.362975e6

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9179
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 177
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variant carriers: 0

GenotypeQuality
all individuals: 489
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 39357
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.851338340073175e-4
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.41e1

DP
type: SiteQuality
SIO_000300: 3.377402e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 39355
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1882
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GenotypeQuality
all individuals: 1008
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9812
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.186e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e0

FS
type: SiteQuality
SIO_000300: 2.444e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.376e1

DP
type: SiteQuality
SIO_000300: 3.385103e6

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.337e0

GenotypeQuality
all individuals: 1009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39356
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
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variant carriers: 0

GenotypeQuality
all individuals: 1160
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variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 2.461e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 4.98e0

QD
type: SiteQuality
SIO_000300: 1.381e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

VQSLOD
type: SiteQuality
SIO_000300: -3.741e0

DP
type: SiteQuality
SIO_000300: 3.38656e6

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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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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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.502268425322237e-5
allele num: 66566
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South Asian
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QD
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DP
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

East Asian
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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FS
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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Latino
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East Asian
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European (Non-Finnish)
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VQSLOD
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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African
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European (Finnish)
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Latino
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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QD
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ClippingRankSum
type: SiteQuality
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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allele num: 11578
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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European (Finnish)
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Latino
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African
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South Asian
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East Asian
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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East Asian
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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African
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MQ
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: -1.552e0

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

African
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allele frequency: 1.926411096127914e-4
allele num: 10382
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.233654083395016e-4
allele num: 16212
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 3.377926e6

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

Latino
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allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506477854775535e-5
allele num: 66380
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 896
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

Latino
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allele frequency: 6.056411143796505e-4
allele num: 11558
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.475e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 3.367253e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.137e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.105e0

QD
type: SiteQuality
SIO_000300: 1.841e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.058e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.184e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.351258e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.934610176049526e-4
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66056
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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FS
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.987e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

African
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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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.597176408497163e-5
allele num: 15158
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Other
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 14888
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 65766
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African
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Other
type: Population
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MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65492
num of homozygotes: 0

Latino
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allele num: 11520
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South Asian
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East Asian
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Other
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.054181174027243e-5
allele num: 65484
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14256
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.465e1

FS
type: SiteQuality
SIO_000300: 2.061e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.280758e6

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.399e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.504e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.028394714647174e-5
allele num: 14228
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.58e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 3.279622e6

VQSLOD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.894e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.278e0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504233979941145e-5
allele num: 66604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.19e1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

DP
type: SiteQuality
SIO_000300: 3.121815e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.697e0

FS
type: SiteQuality
SIO_000300: 6.458e0

MQRankSum
type: SiteQuality
SIO_000300: -1.07e0

DP
type: SiteQuality
SIO_000300: 3.130442e6

VQSLOD
type: SiteQuality
SIO_000300: -6.445e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

QD
type: SiteQuality
SIO_000300: 1.47e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.13057e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.886e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.079e0

QD
type: SiteQuality
SIO_000300: 1.122e1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

FS
type: SiteQuality
SIO_000300: 8.593e0

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeQuality
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bin: 3.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000840235265874e-5
allele num: 66648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 3.131698e6

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.192e0

VQSLOD
type: SiteQuality
SIO_000300: -7.96e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.492e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.656e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.002220821704031e-5
allele num: 66642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.12e1

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

VQSLOD
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SIO_000300: 5.08e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
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

VQSLOD
type: SiteQuality
SIO_000300: 7.5e-1

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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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
allele num: 16312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.129711e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e0

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.221e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.544e1

GenotypeQuality
all individuals: 8710
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.191183754333828e-5
allele num: 16152
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQ
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SIO_000300: 5.932e1

QD
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SIO_000300: 1.142e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

VQSLOD
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SIO_000300: 2.84e0

InbreedingCoeff
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SIO_000300: 1.39e-2

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.064e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
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SIO_000300: 3.124845e6

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

FS
type: SiteQuality
SIO_000300: 2.618e0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

BaseQRankSum
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SIO_000300: -4.543e0

DP
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SIO_000300: 3.123032e6

QD
type: SiteQuality
SIO_000300: 1.014e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504936190705514e-5
allele num: 66448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.02e-1

FS
type: SiteQuality
SIO_000300: 1.691e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.116679e6

GenotypeQuality
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variant carriers: 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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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508659706716553e-5
allele num: 66284
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.736e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.07e-2

DP
type: SiteQuality
SIO_000300: 3.10463e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 1.321e1

FS
type: SiteQuality
SIO_000300: 6.61e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.72e-2

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.93e-1

QD
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
type: Population
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.663440600048391e-4
allele num: 66128
num of homozygotes: 0

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

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

South Asian
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allele frequency: 4.058990664321472e-4
allele num: 14782
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66028
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Other
type: Population
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East Asian
type: Population
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Latino
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allele count: 3
allele frequency: 2.595604775912787e-4
allele num: 11558
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African
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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MQ
type: SiteQuality
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35171
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1552
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2906
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596053997923157e-4
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.770480704129993e-5
allele num: 14770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.850596842510589e-4
allele num: 10388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 5.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

DP
type: SiteQuality
SIO_000300: 3.086214e6

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35171
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2906
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514463122822959e-5
allele num: 66030
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

DP
type: SiteQuality
SIO_000300: 3.086214e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 5.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 2872
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6051
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variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35165
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518233990222573e-5
allele num: 65866
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e0

QD
type: SiteQuality
SIO_000300: 1.143e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

FS
type: SiteQuality
SIO_000300: 2.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.51e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 3.074181e6

GenotypeQuality
all individuals: 2904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2867
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5851
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65734
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13874
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.764e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 3.067499e6

FS
type: SiteQuality
SIO_000300: 3.223e0

QD
type: SiteQuality
SIO_000300: 9.9e0

GenotypeQuality
all individuals: 2901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35164
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2866
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13824
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

QD
type: SiteQuality
SIO_000300: 1.155e1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.939e0

FS
type: SiteQuality
SIO_000300: 5.643e0

DP
type: SiteQuality
SIO_000300: 3.066782e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.019e0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3138
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.303534910896874e-5
allele num: 13692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.828e0

DP
type: SiteQuality
SIO_000300: 3.064954e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.771e0

VQSLOD
type: SiteQuality
SIO_000300: -9.804e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 6.02e0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 80

GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 27

GenotypeQuality
all individuals: 2573
bin: 7.75e1
variant carriers: 109

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 30

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 108

GenotypeQuality
all individuals: 39037
bin: 9.75e1
variant carriers: 24191

GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 104

GenotypeQuality
all individuals: 1445
bin: 8.75e1
variant carriers: 95

GenotypeQuality
all individuals: 294
bin: 2.5e0
variant carriers: 10

GenotypeQuality
all individuals: 1790
bin: 2.25e1
variant carriers: 96

GenotypeQuality
all individuals: 2628
bin: 6.75e1
variant carriers: 52

GenotypeQuality
all individuals: 589
bin: 7.5e0
variant carriers: 20

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 65

GenotypeQuality
all individuals: 2542
bin: 8.25e1
variant carriers: 108

GenotypeQuality
all individuals: 2449
bin: 9.25e1
variant carriers: 45

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 59

Other
type: Population
allele count: 232
allele frequency: 2.703962703962704e-1
allele num: 858
num of homozygotes: 32

European (Finnish)
type: Population
allele count: 1604
allele frequency: 2.425892316999395e-1
allele num: 6612
num of homozygotes: 188

European (Non-Finnish)
type: Population
allele count: 15897
allele frequency: 2.435202205882353e-1
allele num: 65280
num of homozygotes: 1970

Latino
type: Population
allele count: 1591
allele frequency: 1.382036136205698e-1
allele num: 11512
num of homozygotes: 130

East Asian
type: Population
allele count: 1462
allele frequency: 1.695269016697588e-1
allele num: 8624
num of homozygotes: 115

African
type: Population
allele count: 2814
allele frequency: 2.723050125798336e-1
allele num: 10334
num of homozygotes: 361

South Asian
type: Population
allele count: 4764
allele frequency: 3.755912961210974e-1
allele num: 12684
num of homozygotes: 866

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-2

FS
type: SiteQuality
SIO_000300: 6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

DP
type: SiteQuality
SIO_000300: 3.539115e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

QD
type: SiteQuality
SIO_000300: 1.567e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

GenotypeQuality
all individuals: 184
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22823
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3871
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3346
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.079102133817779e-5
allele num: 64954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

FS
type: SiteQuality
SIO_000300: 4.035e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.372e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

DP
type: SiteQuality
SIO_000300: 2.543906e6

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.308e1

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4342
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10974
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.626773596545343e-5
allele num: 64840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.804e0

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

DP
type: SiteQuality
SIO_000300: 2.538299e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1