19-36549656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549656
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549656
    reference: chr 19
allele count: 169
allele frequency: 1.497934799950364e-3
allele num: 112822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.178-26C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.178-26C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.269-26C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.178-26C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.160-26C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.178-26C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.187-26C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25275
  bin: 2.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7559
  bin: 9.75e1
  variant carriers: 168
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3363
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

19-36549667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549667
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549667
    reference: chr 19
allele count: 3
allele frequency: 2.591344908007256e-5
allele num: 115770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.187-15G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.178-15G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.269-15G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.178-15G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.178-15G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.160-15G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.178-15G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34701
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7461
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

19-36549682-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549682
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549682
    reference: chr 19
allele count: 1
allele frequency: 8.446088616361763e-6
allele num: 118398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.178G>A
  hgvsp: ENSP00000465525.1:p.Val60Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.160G>A
  hgvsp: ENSP00000413475.3:p.Val54Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.178G>A
  hgvsp: ENSP00000373651.3:p.Val60Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.269G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.178G>A
  hgvsp: ENSP00000270301.6:p.Val60Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.187G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.178G>A
  hgvsp: ENSP00000384792.1:p.Val60Met
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5772
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1850
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val60Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

19-36549682-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549682
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549682
    reference: chr 19
allele count: 2
allele frequency: 1.689217723272353e-5
allele num: 118398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.178G>T
  hgvsp: ENSP00000270301.6:p.Val60Leu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.269G>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.160G>T
  hgvsp: ENSP00000413475.3:p.Val54Leu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.178G>T
  hgvsp: ENSP00000373651.3:p.Val60Leu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.178G>T
  hgvsp: ENSP00000465525.1:p.Val60Leu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.187G>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.178G>T
  hgvsp: ENSP00000384792.1:p.Val60Leu
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12468
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5772
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val60Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-36549684-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549684
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549684
    reference: chr 19
allele count: 9798
allele frequency: 8.243172754959532e-2
allele num: 118862
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.271G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.180G>A
  hgvsp: ENST00000401500.2:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.162G>A
  hgvsp: ENST00000427823.2:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.180G>A
  hgvsp: ENST00000587391.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.189G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.180G>A
  hgvsp: ENST00000270301.7:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.180G>A
  hgvsp: ENST00000388999.3:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.25e1
  variant carriers: 964
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.75e1
  variant carriers: 328
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 9.75e1
  variant carriers: 1595
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 609
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 1.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 12423
  bin: 2.75e1
  variant carriers: 1210
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 385
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 3.25e1
  variant carriers: 1353
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 3.75e1
  variant carriers: 1254
genotype depth: GenotypeDepth
  all individuals: 29161
  bin: 2.25e1
  variant carriers: 716
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 8.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 9.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.25e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.75e1
  variant carriers: 3
hgvs: c.180G>A
num of homozygotes: 724
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-36549690-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549690
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549690
    reference: chr 19
allele count: 1
allele frequency: 8.329446258412741e-6
allele num: 120056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.186C>A
  hgvsp: ENST00000270301.7:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.277C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.186C>A
  hgvsp: ENST00000401500.2:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.168C>A
  hgvsp: ENST00000427823.2:c.168C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.186C>A
  hgvsp: ENST00000388999.3:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.186C>A
  hgvsp: ENST00000587391.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.195C>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu62Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

19-36549690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549690
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549690
    reference: chr 19
allele count: 21548
allele frequency: 1.794829079762778e-1
allele num: 120056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.186C>T
  hgvsp: ENST00000270301.7:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.186C>T
  hgvsp: ENST00000388999.3:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.195C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.186C>T
  hgvsp: ENST00000401500.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.186C>T
  hgvsp: ENST00000587391.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.277C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.168C>T
  hgvsp: ENST00000427823.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 326
genotype depth: GenotypeDepth
  all individuals: 21306
  bin: 2.25e1
  variant carriers: 1328
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.25e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 527
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 3.75e1
  variant carriers: 2759
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 622
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 1196
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 2668
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 4.25e1
  variant carriers: 2274
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 2.75e1
  variant carriers: 2183
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 9.75e1
  variant carriers: 2349
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 838
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.75e1
  variant carriers: 1685
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 189
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 8.25e1
  variant carriers: 122
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.75e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 9.25e1
  variant carriers: 116
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.25e1
  variant carriers: 74
genotype quality: GenotypeQuality
  all individuals: 23073
  bin: 9.75e1
  variant carriers: 18440
hgvs: p.Leu62Leu
num of homozygotes: 2083
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-36549693-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549693
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549693
    reference: chr 19
allele count: 73
allele frequency: 6.068970104086994e-4
allele num: 120284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.280G>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.189G>T
  hgvsp: ENSP00000465525.1:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.198G>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.189G>T
  hgvsp: ENSP00000373651.3:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.171G>T
  hgvsp: ENSP00000413475.3:p.Glu57Asp
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.189G>T
  hgvsp: ENSP00000384792.1:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.189G>T
  hgvsp: ENSP00000270301.6:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24084
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20315
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7231
  bin: 9.75e1
  variant carriers: 72
hgvs: p.Glu63Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/19-36549700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549700
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549700
    reference: chr 19
allele count: 2
allele frequency: 1.660688189185599e-5
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.196C>A
  hgvsp: ENSP00000384792.1:p.Leu66Ile
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.287C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.196C>A
  hgvsp: ENSP00000373651.3:p.Leu66Ile
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.196C>A
  hgvsp: ENSP00000270301.6:p.Leu66Ile
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.178C>A
  hgvsp: ENSP00000413475.3:p.Leu60Ile
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.196C>A
  hgvsp: ENSP00000465525.1:p.Leu66Ile
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.205C>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6061
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7154
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41081
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu66Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

19-36549707-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549707
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549707
    reference: chr 19
allele count: 13
allele frequency: 1.078533857666716e-4
allele num: 120534
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.185T>C
  hgvsp: ENSP00000413475.3:p.Ile62Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.203T>C
  hgvsp: ENSP00000384792.1:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.294T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.203T>C
  hgvsp: ENSP00000373651.3:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.203T>C
  hgvsp: ENSP00000465525.1:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.212T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.203T>C
  hgvsp: ENSP00000270301.6:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile68Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

19-36549717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549717
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549717
    reference: chr 19
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.213G>A
  hgvsp: ENST00000401500.2:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.213G>A
  hgvsp: ENST00000388999.3:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.222G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.195G>A
  hgvsp: ENST00000427823.2:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.213G>A
  hgvsp: ENST00000587391.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.213G>A
  hgvsp: ENST00000270301.7:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.304G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln71Gln
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-36549720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549720
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549720
    reference: chr 19
allele count: 3
allele frequency: 2.488387524883875e-5
allele num: 120560
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.216C>T
  hgvsp: ENST00000401500.2:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.198C>T
  hgvsp: ENST00000427823.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.307C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.225C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.216C>T
  hgvsp: ENST00000270301.7:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.216C>T
  hgvsp: ENST00000587391.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.216C>T
  hgvsp: ENST00000388999.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn72Asn
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: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-36549723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549723
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549723
    reference: chr 19
allele count: 2
allele frequency: 1.659227795384028e-5
allele num: 120538
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.219C>T
  hgvsp: ENST00000401500.2:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.228C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.219C>T
  hgvsp: ENST00000388999.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.219C>T
  hgvsp: ENST00000270301.7:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.201C>T
  hgvsp: ENST00000427823.2:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.310C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.219C>T
  hgvsp: ENST00000587391.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5983
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser73Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

19-36549724-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549724
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549724
    reference: chr 19
allele count: 8
allele frequency: 6.636690945894378e-5
allele num: 120542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.220A>G
  hgvsp: ENSP00000373651.3:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.202A>G
  hgvsp: ENSP00000413475.3:p.Ser68Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.220A>G
  hgvsp: ENSP00000465525.1:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.220A>G
  hgvsp: ENSP00000270301.6:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.229A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.220A>G
  hgvsp: ENSP00000384792.1:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.311A>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24444
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5989
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser74Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

19-36549726-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549726
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549726
    reference: chr 19
allele count: 5
allele frequency: 4.151237899141524e-5
allele num: 120446
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.222T>C
  hgvsp: ENST00000270301.7:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.222T>C
  hgvsp: ENST00000388999.3:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.222T>C
  hgvsp: ENST00000401500.2:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.231T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.204T>C
  hgvsp: ENST00000427823.2:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.313T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.222T>C
  hgvsp: ENST00000587391.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20900
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24247
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser74Ser
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/19-36549735-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549735
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549735
    reference: chr 19
allele count: 2
allele frequency: 1.6628421297682e-5
allele num: 120276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.231C>A
  hgvsp: ENST00000587391.1:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.213C>A
  hgvsp: ENST00000427823.2:c.213C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.322C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.231C>A
  hgvsp: ENST00000401500.2:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.240C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.231C>A
  hgvsp: ENST00000388999.3:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.231C>A
  hgvsp: ENST00000270301.7:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr77Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

19-36549745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549745
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549745
    reference: chr 19
allele count: 14
allele frequency: 1.167912439935932e-4
allele num: 119872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.250G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.241G>A
  hgvsp: ENSP00000465525.1:p.Gly81Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.241G>A
  hgvsp: ENSP00000373651.3:p.Gly81Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.223G>A
  hgvsp: ENSP00000413475.3:p.Gly75Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.241G>A
  hgvsp: ENSP00000384792.1:p.Gly81Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.332G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.241G>A
  hgvsp: ENSP00000270301.6:p.Gly81Ser
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20771
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23532
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41083
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5756
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly81Ser
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

19-36549757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549757
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549757
    reference: chr 19
allele count: 143
allele frequency: 1.205570917920011e-3
allele num: 118616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.253G>A
  hgvsp: ENSP00000270301.6:p.Val85Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.262G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.253G>A
  hgvsp: ENSP00000373651.3:p.Val85Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.344G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.253G>A
  hgvsp: ENSP00000465525.1:p.Val85Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.235G>A
  hgvsp: ENSP00000413475.3:p.Val79Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.253G>A
  hgvsp: ENSP00000384792.1:p.Val85Met
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20255
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22341
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7224
  bin: 9.75e1
  variant carriers: 142
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 9.25e1
  variant carriers: 1
hgvs: p.Val85Met
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-36549764-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549764
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549764
    reference: chr 19
allele count: 1
allele frequency: 8.534607834769993e-6
allele num: 117170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.260A>G
  hgvsp: ENSP00000270301.6:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.351A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.242A>G
  hgvsp: ENSP00000413475.3:p.Tyr81Cys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.260A>G
  hgvsp: ENSP00000465525.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.269A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.260A>G
  hgvsp: ENSP00000373651.3:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.260A>G
  hgvsp: ENSP00000384792.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21230
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7090
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37746
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5137
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr87Cys
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36549775-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549775
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549775
    reference: chr 19
allele count: 2
allele frequency: 1.770851779706039e-5
allele num: 112940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+2T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+2T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+2T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+2T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+2T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+2T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+2T>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7082
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8575
  bin: 2.25e1
  variant carriers: 0
hgvs: c.269+2T>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36549777-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549777
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549777
    reference: chr 19
allele count: 1
allele frequency: 8.864148066729306e-6
allele num: 112814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+4A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+4A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+4A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+4A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+4A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+4A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+4A>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4146
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 2.75e1
  variant carriers: 0
hgvs: c.269+4A>G
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

19-36549783-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549783
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549782
    reference: chr 19
allele count: 1208
allele frequency: 1.103861688323556e-2
allele num: 109434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+12delA
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+12delA
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+12delA
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+12delA
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+12delA
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+12delA
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+12delA
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14049
  bin: 2.75e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 1.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 11348
  bin: 1.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 2.25e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 3.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 9.75e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3321
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2660
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 12
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: TA
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

19-36549784-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549784
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549784
    reference: chr 19
allele count: 1
allele frequency: 9.42400482509047e-6
allele num: 106112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+11A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+11A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+11A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+11A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+11A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+11A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+11A>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-36549792-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549792
    reference: chr 19
allele count: 1
allele frequency: 9.544534799373879e-6
allele num: 104772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+19C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+19C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+19C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+19C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+19C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+19C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+19C>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10502
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7203
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

19-36549792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549792
    reference: chr 19
allele count: 105
allele frequency: 1.002176153934257e-3
allele num: 104772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+19C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+19C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+19C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+19C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+19C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+19C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+19C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10502
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17884
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

19-36549795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549795
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549795
    reference: chr 19
allele count: 2
allele frequency: 1.928528725435365e-5
allele num: 103706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+22C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+22C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+22C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+22C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+22C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+22C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+22C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4594
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36549796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549796
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549796
    reference: chr 19
allele count: 1
allele frequency: 9.697063729102828e-6
allele num: 103124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+23G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+23G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+23G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+23G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+23G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+23G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+23G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19639
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4691
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-36549804-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549804
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549804
    reference: chr 19
allele count: 5
allele frequency: 5.003903044374612e-5
allele num: 99922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+31A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+31A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+31A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+31A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+31A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+31A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+31A>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8751
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7117
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17091
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

19-36549806-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549806
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549806
    reference: chr 19
allele count: 3
allele frequency: 3.021756647864625e-5
allele num: 99280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+33T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+33T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+33T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+33T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+33T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+33T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+33T>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21072
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16857
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1836
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-36549813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549813
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549813
    reference: chr 19
allele count: 4
allele frequency: 4.1583499667332e-5
allele num: 96192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+40G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+40G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+40G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.251+40G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+40G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+40G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+40G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10256
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11079
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1328
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7956
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5466
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-36549830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549830
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549830
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 59558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+57C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+57C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+57C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-49C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+57C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+57C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+57C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20019
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4089
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-36549836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549836
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549836
    reference: chr 19
allele count: 1
allele frequency: 1.881892431028642e-5
allele num: 53138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+63G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+63G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+63G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+63G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+63G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-43G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+63G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13754
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15039
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

19-36549842-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549842
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549842
    reference: chr 19
allele count: 3
allele frequency: 6.872852233676975e-5
allele num: 43650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+69C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+69C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+69C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+69C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+69C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+69C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-37C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11266
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22647
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-36549843-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549843
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549843
    reference: chr 19
allele count: 32
allele frequency: 7.556794030132716e-4
allele num: 42346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+70G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+70G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+70G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+70G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+70G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+70G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-36G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16771
  bin: 7.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10819
  bin: 1.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20279
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4647
  bin: 9.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21927
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-36549849-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549849
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549849
    reference: chr 19
allele count: 2
allele frequency: 6.180087757246153e-5
allele num: 32362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+76C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-30C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+76C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+76C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+76C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+76C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+76C>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26099
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4616
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27292
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

19-36549862-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549862
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549862
    reference: chr 19
allele count: 59
allele frequency: 2.422798948751643e-3
allele num: 24352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+89A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+89A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-17A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+89A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+89A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+89A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+89A>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31507
  bin: 2.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10321
  bin: 7.5e0
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8639
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 4667
  bin: 9.75e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31827
  bin: 7.5e0
  variant carriers: 4
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: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

19-36549865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549865
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549865
    reference: chr 19
allele count: 70
allele frequency: 2.978216473791695e-3
allele num: 23504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.252-14T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+92T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+92T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+92T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+92T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+92T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+92T>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32099
  bin: 2.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 7.5e0
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32451
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 1.75e1
  variant carriers: 5
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

19-36549881-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549881
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549881
    reference: chr 19
allele count: 2
allele frequency: 1.010305112143867e-4
allele num: 19796
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+108T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.254T>C
  hgvsp: ENSP00000413475.3:p.Met85Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+108T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+108T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+108T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+108T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+108T>C
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31104
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2534
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met85Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

19-36549898-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549898
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549898
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 18748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+125G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+125G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+125G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.271G>C
  hgvsp: ENSP00000413475.3:p.Ala91Pro
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+125G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+125G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+125G>C
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4562
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala91Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

19-36549911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549911
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549911
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 18368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+138G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+138G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+138G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+138G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.284G>A
  hgvsp: ENSP00000413475.3:p.Cys95Tyr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+138G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+138G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21884
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys95Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-36549911-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549911
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549911
    reference: chr 19
allele count: 1
allele frequency: 5.444250871080139e-5
allele num: 18368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+138G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+138G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+138G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+138G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.284G>C
  hgvsp: ENSP00000413475.3:p.Cys95Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+138G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+138G>C
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21884
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20352
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys95Ser
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-36549930-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549930
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549930
    reference: chr 19
allele count: 1
allele frequency: 5.670220004536176e-5
allele num: 17636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+157C>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+157C>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+157C>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+157C>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.303C>G
  hgvsp: ENST00000427823.2:c.303C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+157C>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+157C>G
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15434
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13869
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala101Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/19-36549952-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549952
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549952
    reference: chr 19
allele count: 1
allele frequency: 5.813277525869085e-5
allele num: 17202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+179C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.325C>A
  hgvsp: ENSP00000413475.3:p.Pro109Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+179C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+179C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+179C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+179C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+179C>A
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro109Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-36549953-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549953
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549953
    reference: chr 19
allele count: 1
allele frequency: 5.82682671017364e-5
allele num: 17162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+180C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+180C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.326C>A
  hgvsp: ENSP00000413475.3:p.Pro109His
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+180C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+180C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+180C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+180C>A
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro109His
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

19-36549972-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549972
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549972
    reference: chr 19
allele count: 1
allele frequency: 5.953798523457966e-5
allele num: 16796
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+199A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+199A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+199A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.335+10A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+199A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+199A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+199A>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6581
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

19-36549978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549978
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549978
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 16696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+205G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+205G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.335+16G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+205G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+205G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+205G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+205G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5650
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-36549995-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549995
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549995
    reference: chr 19
allele count: 1
allele frequency: 6.040836051709557e-5
allele num: 16554
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+222A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+222A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+222A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+222A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+222A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+222A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.335+33A>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-36549997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549997
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549997
    reference: chr 19
allele count: 1
allele frequency: 6.044487427466151e-5
allele num: 16544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+224G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+224G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+224G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+224G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+224G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.335+35G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+224G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4553
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4287
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

19-36549997-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36549997
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36549997
    reference: chr 19
allele count: 33
allele frequency: 1.99468085106383e-3
allele num: 16544
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.269+224G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.278+224G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.360+224G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.335+35G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.269+224G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.269+224G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.269+224G>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4287
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-36550819-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550819
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550819
    reference: chr 19
allele count: 15
allele frequency: 1.235584843492587e-4
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.270-51A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.336-51A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.270-51A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.270-51A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.279-51A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.361-51A>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.270-51A>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51867
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-36550839-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550839
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550839
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.270-31A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.270-31A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.270-31A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.279-31A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.361-31A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.270-31A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.336-31A>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51865
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

19-36550841-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550841
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550841
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.361-29T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.336-29T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.270-29T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.270-29T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.279-29T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.270-29T>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.270-29T>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51865
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

19-36550849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550849
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550849
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.270-21C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.270-21C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.279-21C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.270-21C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.361-21C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.336-21C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.270-21C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

19-36550858-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550858
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550856
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.270-10_270-9delTT
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.336-10_336-9delTT
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.270-10_270-9delTT
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.270-10_270-9delTT
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.279-10_279-9delTT
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.361-10_361-9delTT
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.270-10_270-9delTT
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51865
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: CTT
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

19-36550877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550877
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550877
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.277G>A
  hgvsp: ENSP00000270301.6:p.Val93Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.343G>A
  hgvsp: ENSP00000413475.3:p.Val115Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.368G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.277G>A
  hgvsp: ENSP00000384792.1:p.Val93Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.277G>A
  hgvsp: ENSP00000465525.1:p.Val93Met
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.286G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.277G>A
  hgvsp: ENSP00000373651.3:p.Val93Met
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val93Met
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

19-36550890-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550890
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550890
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.290A>G
  hgvsp: ENSP00000465525.1:p.Asp97Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.299A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.290A>G
  hgvsp: ENSP00000270301.6:p.Asp97Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.356A>G
  hgvsp: ENSP00000413475.3:p.Asp119Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.290A>G
  hgvsp: ENSP00000373651.3:p.Asp97Gly
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.381A>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.290A>G
  hgvsp: ENSP00000384792.1:p.Asp97Gly
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp97Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-36550891-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550891
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550891
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.291C>T
  hgvsp: ENST00000270301.7:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.357C>T
  hgvsp: ENST00000427823.2:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.382C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.291C>T
  hgvsp: ENST00000401500.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.291C>T
  hgvsp: ENST00000388999.3:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.300C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.291C>T
  hgvsp: ENST00000587391.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51865
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp97Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-36550902-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550902
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550902
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.311A>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.302A>C
  hgvsp: ENSP00000373651.3:p.Asn101Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.302A>C
  hgvsp: ENSP00000465525.1:p.Asn101Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.368A>C
  hgvsp: ENSP00000413475.3:p.Asn123Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.302A>C
  hgvsp: ENSP00000384792.1:p.Asn101Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.302A>C
  hgvsp: ENSP00000270301.6:p.Asn101Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.393A>C
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn101Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/19-36550903-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550903
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550903
    reference: chr 19
allele count: 21
allele frequency: 1.729676303434643e-4
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.312C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.303C>A
  hgvsp: ENSP00000384792.1:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.303C>A
  hgvsp: ENSP00000465525.1:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.369C>A
  hgvsp: ENSP00000413475.3:p.Asn123Lys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.303C>A
  hgvsp: ENSP00000373651.3:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.394C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.303C>A
  hgvsp: ENSP00000270301.6:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  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: 51867
  bin: 9.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn101Lys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

19-36550910-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550910
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550910
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.319C>G
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.310C>G
  hgvsp: ENSP00000465525.1:p.Gln104Glu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.310C>G
  hgvsp: ENSP00000270301.6:p.Gln104Glu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.376C>G
  hgvsp: ENSP00000413475.3:p.Gln126Glu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.310C>G
  hgvsp: ENSP00000373651.3:p.Gln104Glu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.310C>G
  hgvsp: ENSP00000384792.1:p.Gln104Glu
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.401C>G
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln104Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

19-36550912-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550912
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550912
    reference: chr 19
allele count: 66
allele frequency: 5.436125525080306e-4
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.321G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.378G>C
  hgvsp: ENSP00000413475.3:p.Gln126His
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.312G>C
  hgvsp: ENSP00000465525.1:p.Gln104His
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.312G>C
  hgvsp: ENSP00000373651.3:p.Gln104His
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.403G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.312G>C
  hgvsp: ENSP00000270301.6:p.Gln104His
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.312G>C
  hgvsp: ENSP00000384792.1:p.Gln104His
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 9.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln104His
num of homozygotes: 1
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-36550912-GCAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550912
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550909
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.313_315delCAC
  hgvsp: ENSP00000270301.6:p.His105del
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.313_315delCAC
  hgvsp: ENSP00000373651.3:p.His105del
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.379_381delCAC
  hgvsp: ENSP00000413475.3:p.His127del
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.313_315delCAC
  hgvsp: ENSP00000384792.1:p.His105del
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.313_315delCAC
  hgvsp: ENSP00000465525.1:p.His105del
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.404_406delCAC
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.322_324delCAC
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51862
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His105del
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: GCAC
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/19-36550918-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550918
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550918
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.318C>A
  hgvsp: ENST00000587391.1:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.384C>A
  hgvsp: ENST00000427823.2:c.384C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.409C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.318C>A
  hgvsp: ENST00000388999.3:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.318C>A
  hgvsp: ENST00000270301.7:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.327C>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.318C>A
  hgvsp: ENST00000401500.2:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile106Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

19-36550924-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550924
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550924
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.324C>T
  hgvsp: ENST00000270301.7:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.415C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.390C>T
  hgvsp: ENST00000427823.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.333C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.324C>T
  hgvsp: ENST00000587391.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.324C>T
  hgvsp: ENST00000401500.2:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.324C>T
  hgvsp: ENST00000388999.3:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn108Asn
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

19-36550927-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550927
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550927
    reference: chr 19
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.327C>T
  hgvsp: ENST00000270301.7:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.327C>T
  hgvsp: ENST00000587391.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.336C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.418C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.327C>T
  hgvsp: ENST00000401500.2:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.393C>T
  hgvsp: ENST00000427823.2:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.327C>T
  hgvsp: ENST00000388999.3:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr109Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-36550928-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550928
    reference: chr 19
allele count: 6
allele frequency: 4.942257952916756e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.328G>A
  hgvsp: ENSP00000465525.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.419G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.394G>A
  hgvsp: ENSP00000413475.3:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.328G>A
  hgvsp: ENSP00000373651.3:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.328G>A
  hgvsp: ENSP00000384792.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.328G>A
  hgvsp: ENSP00000270301.6:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.337G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala110Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

19-36550928-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550928
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.394G>T
  hgvsp: ENSP00000413475.3:p.Ala132Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.328G>T
  hgvsp: ENSP00000373651.3:p.Ala110Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.419G>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.337G>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.328G>T
  hgvsp: ENSP00000465525.1:p.Ala110Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.328G>T
  hgvsp: ENSP00000270301.6:p.Ala110Ser
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.328G>T
  hgvsp: ENSP00000384792.1:p.Ala110Ser
  variant of: http://identifiers.org/hgnc/24502
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51851
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala110Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

19-36550952-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550952
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550952
    reference: chr 19
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.332+20C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.332+20C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.398+20C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.332+20C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.332+20C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.361C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.423+20C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

19-36550953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550953
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550953
    reference: chr 19
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.362G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.332+21G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.423+21G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.332+21G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.398+21G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.332+21G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.332+21G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-36550957-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550957
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550957
    reference: chr 19
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.332+25C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.423+25C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.398+25C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.366C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.332+25C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.332+25C>T
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.332+25C>T
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

19-36550962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550962
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550962
    reference: chr 19
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.332+30G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.371G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.332+30G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.332+30G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.423+30G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.398+30G>A
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.332+30G>A
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51845
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

19-36550962-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36550962
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 36550962
    reference: chr 19
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000270301
  ensembl transcript: ENST00000270301
  gene symbol: WDR62
  hgvsc: ENST00000270301.7:c.332+30G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000373651
  ensembl transcript: ENST00000388999
  gene symbol: WDR62
  hgvsc: ENST00000388999.3:c.332+30G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000384792
  ensembl transcript: ENST00000401500
  gene symbol: WDR62
  hgvsc: ENST00000401500.2:c.332+30G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000465525
  ensembl transcript: ENST00000587391
  gene symbol: WDR62
  hgvsc: ENST00000587391.1:c.332+30G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl protein: ENSP00000413475
  ensembl transcript: ENST00000427823
  gene symbol: WDR62
  hgvsc: ENST00000427823.2:c.398+30G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000608676
  gene symbol: WDR62
  hgvsc: ENST00000608676.1:n.371G>C
  variant of: http://identifiers.org/hgnc/24502
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075702
  ensembl transcript: ENST00000378860
  gene symbol: WDR62
  hgvsc: ENST00000378860.4:n.423+30G>C
  variant of: http://identifiers.org/hgnc/24502
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1456
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27745
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4920
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 148
allele frequency: 1.876267748478702e-2
allele num: 7888
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.262785705265816e-3
allele num: 15838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61848
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.201923076923077e-3
allele num: 832
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.861528e6

FS
type: SiteQuality
SIO_000300: 3.381e0

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5291
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.723368076329628e-5
allele num: 63514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.077e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 3.256e0

VQSLOD
type: SiteQuality
SIO_000300: -1.523e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.339e0

DP
type: SiteQuality
SIO_000300: 1.949632e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.99e-1

GenotypeQuality
all individuals: 1621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7534
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.159152500615915e-5
allele num: 16236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

FS
type: SiteQuality
SIO_000300: 9.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.975e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

DP
type: SiteQuality
SIO_000300: 2.004037e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.903e0

GenotypeQuality
all individuals: 567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7534
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.076165866863541e-5
allele num: 65016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 2.004037e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.903e0

FS
type: SiteQuality
SIO_000300: 9.69e0

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.975e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1305
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 424
bin: 3.25e1
variant carriers: 9

GenotypeQuality
all individuals: 4877
bin: 6.75e1
variant carriers: 49

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 17

GenotypeQuality
all individuals: 14423
bin: 9.75e1
variant carriers: 8705

GenotypeQuality
all individuals: 32972
bin: 6.25e1
variant carriers: 31

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 369
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1494
bin: 7.25e1
variant carriers: 26

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 25

GenotypeQuality
all individuals: 1560
bin: 7.75e1
variant carriers: 46

African
type: Population
allele count: 253
allele frequency: 2.514910536779324e-2
allele num: 10060
num of homozygotes: 0

South Asian
type: Population
allele count: 3336
allele frequency: 2.039618488628026e-1
allele num: 16356
num of homozygotes: 384

Other
type: Population
allele count: 62
allele frequency: 7.029478458049887e-2
allele num: 882
num of homozygotes: 3

Latino
type: Population
allele count: 1246
allele frequency: 1.099929378531073e-1
allele num: 11328
num of homozygotes: 59

European (Non-Finnish)
type: Population
allele count: 2747
allele frequency: 4.211639887158102e-2
allele num: 65224
num of homozygotes: 62

European (Finnish)
type: Population
allele count: 231
allele frequency: 3.556034482758621e-2
allele num: 6496
num of homozygotes: 3

East Asian
type: Population
allele count: 1923
allele frequency: 2.258102395490841e-1
allele num: 8516
num of homozygotes: 213

DP
type: SiteQuality
SIO_000300: 2.284548e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.28e-2

QD
type: SiteQuality
SIO_000300: 1.316e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 5.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.716e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23073
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3680
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 1
allele frequency: 8.750437521876094e-5
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.397e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

FS
type: SiteQuality
SIO_000300: 5.669999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.42e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e0

DP
type: SiteQuality
SIO_000300: 2.584861e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

GenotypeQuality
all individuals: 633
bin: 2.25e1
variant carriers: 16

GenotypeQuality
all individuals: 216
bin: 3.75e1
variant carriers: 29

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 33

GenotypeQuality
all individuals: 28435
bin: 6.25e1
variant carriers: 86

GenotypeQuality
all individuals: 3680
bin: 6.75e1
variant carriers: 119

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 90

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 62

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 11

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 22

GenotypeQuality
all individuals: 889
bin: 7.25e1
variant carriers: 52

GenotypeQuality
all individuals: 895
bin: 7.75e1
variant carriers: 142

European (Finnish)
type: Population
allele count: 1122
allele frequency: 1.710887465690759e-1
allele num: 6558
num of homozygotes: 103

East Asian
type: Population
allele count: 1671
allele frequency: 1.940766550522648e-1
allele num: 8610
num of homozygotes: 139

South Asian
type: Population
allele count: 2924
allele frequency: 1.778588807785888e-1
allele num: 16440
num of homozygotes: 302

European (Non-Finnish)
type: Population
allele count: 13613
allele frequency: 2.063763985324884e-1
allele num: 65962
num of homozygotes: 1400

Latino
type: Population
allele count: 1658
allele frequency: 1.450822541127056e-1
allele num: 11428
num of homozygotes: 112

Other
type: Population
allele count: 164
allele frequency: 1.846846846846847e-1
allele num: 888
num of homozygotes: 16

African
type: Population
allele count: 396
allele frequency: 3.893805309734513e-2
allele num: 10170
num of homozygotes: 11

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 5.669999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.42e1

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

DP
type: SiteQuality
SIO_000300: 2.584861e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.397e0

GenotypeQuality
all individuals: 695
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

East Asian
type: Population
allele count: 73
allele frequency: 8.466713059614939e-3
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66072
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.288e1

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 2.753e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.423e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.133298e6

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

DP
type: SiteQuality
SIO_000300: 2.135416e6

FS
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.434e1

GenotypeQuality
all individuals: 138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6089
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41554
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7156
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 603
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.265329959120109e-3
allele num: 10274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 3.326e0

QD
type: SiteQuality
SIO_000300: 1.225e1

DP
type: SiteQuality
SIO_000300: 2.138079e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.43e-1

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7138
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 687
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41946
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
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: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66218
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.399999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.229000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.140619e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.962e0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7140
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42046
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.530900743067722e-5
allele num: 66212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.281e1

FS
type: SiteQuality
SIO_000300: 6.677e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.182e0

DP
type: SiteQuality
SIO_000300: 2.140724e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 113
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66190
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.502e0

MQ
type: SiteQuality
SIO_000300: 5.859e1

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

DP
type: SiteQuality
SIO_000300: 2.140672e6

FS
type: SiteQuality
SIO_000300: 4.594e0

VQSLOD
type: SiteQuality
SIO_000300: -2.494e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.947e1

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 2.25e1
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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bin: 6.25e1
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GenotypeQuality
all individuals: 7141
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
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variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.208605269518975e-4
allele num: 66192
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

FS
type: SiteQuality
SIO_000300: 2.876e0

DP
type: SiteQuality
SIO_000300: 2.140384e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.131e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 41753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 377
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GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 190
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 7139
bin: 9.75e1
variant carriers: 5

African
type: Population
allele count: 5
allele frequency: 4.864759680871765e-4
allele num: 10278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66150
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.435e0

QD
type: SiteQuality
SIO_000300: 1.883e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e-1

DP
type: SiteQuality
SIO_000300: 2.139077e6

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7137
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 41670
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variant carriers: 0

GenotypeQuality
all individuals: 374
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GenotypeQuality
all individuals: 121
bin: 4.75e1
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GenotypeQuality
all individuals: 1417
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GenotypeQuality
all individuals: 270
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variant carriers: 0

GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 5883
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variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027367401307823e-5
allele num: 66064
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
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: 6590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.113e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.888e0

DP
type: SiteQuality
SIO_000300: 2.135643e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 7135
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variant carriers: 14

GenotypeQuality
all individuals: 260
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GenotypeQuality
all individuals: 313
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GenotypeQuality
all individuals: 365
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GenotypeQuality
all individuals: 1349
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GenotypeQuality
all individuals: 163
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GenotypeQuality
all individuals: 284
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variant carriers: 0

GenotypeQuality
all individuals: 292
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variant carriers: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.279962764719572e-3
allele num: 8594
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.771350400625366e-5
allele num: 10234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038590094196293e-5
allele num: 65820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.062e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

DP
type: SiteQuality
SIO_000300: 2.127449e6

FS
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

GenotypeQuality
all individuals: 1228
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variant carriers: 0

GenotypeQuality
all individuals: 135
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GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 193
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 247
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GenotypeQuality
all individuals: 293
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.170554115759595e-5
allele num: 16206
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.66998932004272e-4
allele num: 11236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 127
allele frequency: 1.948869042138539e-3
allele num: 65166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.666360012266176e-4
allele num: 6522
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.932065755595167e-4
allele num: 10098
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.431e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

DP
type: SiteQuality
SIO_000300: 2.103532e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-3

QD
type: SiteQuality
SIO_000300: 1.299e1

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-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
all individuals: 1145
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GenotypeQuality
all individuals: 1001
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variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
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African
type: Population
allele count: 1
allele frequency: 1.000400160064026e-4
allele num: 9996
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.407e0

QD
type: SiteQuality
SIO_000300: 7.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

FS
type: SiteQuality
SIO_000300: 9.565e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 2.072035e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 50
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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
all individuals: 857
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GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.220715643015878e-5
allele num: 62098
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.981958e6

QD
type: SiteQuality
SIO_000300: 1.572e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 234
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 7081
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1755
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GenotypeQuality
all individuals: 896
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GenotypeQuality
all individuals: 330
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variant carriers: 0

GenotypeQuality
all individuals: 32161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.505703422053231e-5
allele num: 10520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.153e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.13e-1

QD
type: SiteQuality
SIO_000300: 1.553e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.982407e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 1347
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2860
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 762
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7910
bin: 9.75e1
variant carriers: 1188

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 497
allele frequency: 8.269825950946786e-3
allele num: 60098
num of homozygotes: 1

Latino
type: Population
allele count: 34
allele frequency: 3.392536419876272e-3
allele num: 10022
num of homozygotes: 0

South Asian
type: Population
allele count: 645
allele frequency: 4.211832310304297e-2
allele num: 15314
num of homozygotes: 10

Other
type: Population
allele count: 13
allele frequency: 1.585365853658537e-2
allele num: 820
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.956947162426614e-3
allele num: 6132
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.2999788000848e-4
allele num: 9434
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.626740215392698e-4
allele num: 7614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

FS
type: SiteQuality
SIO_000300: 6.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

DP
type: SiteQuality
SIO_000300: 1.896908e6

QD
type: SiteQuality
SIO_000300: 1.53e1

MQ
type: SiteQuality
SIO_000300: 6.032e1

GenotypeQuality
all individuals: 3103
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23454
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7494
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.06951871657754e-4
allele num: 9350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.893e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 1.779708e6

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

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

GenotypeQuality
all individuals: 617
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16701
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4277
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7146
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.701514542286557e-5
allele num: 14922
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

DP
type: SiteQuality
SIO_000300: 1.728614e6

QD
type: SiteQuality
SIO_000300: 1.422e1

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

GenotypeQuality
all individuals: 7203
bin: 9.75e1
variant carriers: 101

GenotypeQuality
all individuals: 16701
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 700
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 1

Other
type: Population
allele count: 1
allele frequency: 1.269035532994924e-3
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

African
type: Population
allele count: 59
allele frequency: 6.473557164801405e-3
allele num: 9114
num of homozygotes: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.701514542286557e-5
allele num: 14922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 4.358134021337424e-4
allele num: 57364
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.79876854184159e-4
allele num: 7146
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.795142555438226e-3
allele num: 9470
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

DP
type: SiteQuality
SIO_000300: 1.728614e6

QD
type: SiteQuality
SIO_000300: 1.422e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.58e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5803
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17020
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7113
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 344
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.761928254281486e-5
allele num: 56756
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14844
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.108647450110865e-4
allele num: 9020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.273e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e0

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.693054e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeQuality
all individuals: 950
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14231
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6051
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 340
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7114
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.772044230223986e-5
allele num: 56432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14778
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 1.716e0

DP
type: SiteQuality
SIO_000300: 1.681136e6

QD
type: SiteQuality
SIO_000300: 1.471e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

GenotypeQuality
all individuals: 618
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5324
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.441156228492773e-4
allele num: 14530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54572
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

QD
type: SiteQuality
SIO_000300: 1.456e1

FS
type: SiteQuality
SIO_000300: 1.192e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.088e0

DP
type: SiteQuality
SIO_000300: 1.600495e6

VQSLOD
type: SiteQuality
SIO_000300: 4.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

GenotypeQuality
all individuals: 392
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4794
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7778
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7118
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 530
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.535259603675413e-5
allele num: 54198
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 9.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.881e0

DP
type: SiteQuality
SIO_000300: 1.590875e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

GenotypeQuality
all individuals: 2287
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5749
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7117
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 6.377551020408163e-4
allele num: 6272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.019e1

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.839e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

DP
type: SiteQuality
SIO_000300: 1.559283e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 10870
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1202
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4617
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10958
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.76429e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.28e-2

FS
type: SiteQuality
SIO_000300: 7.005e0

QD
type: SiteQuality
SIO_000300: 9.07e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

GenotypeQuality
all individuals: 4617
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1222
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.652834599649328e-5
allele num: 27376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2866
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

QD
type: SiteQuality
SIO_000300: 1.576e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.24454e5

VQSLOD
type: SiteQuality
SIO_000300: -9.660000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4617
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 971
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21222
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.579593332112108e-5
allele num: 21836
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 9.46969696969697e-4
allele num: 2112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3082
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 7.54228e5

VQSLOD
type: SiteQuality
SIO_000300: -2.442e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.149e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 1168
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22122
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 926
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2704
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 4

East Asian
type: Population
allele count: 30
allele frequency: 1.489572989076465e-2
allele num: 2014
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2192
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 9.503896597605019e-5
allele num: 21044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.35e-2

FS
type: SiteQuality
SIO_000300: 6.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

DP
type: SiteQuality
SIO_000300: 7.45083e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1779
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15440
bin: 2.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.639344262295082e-3
allele num: 1220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.186e0

DP
type: SiteQuality
SIO_000300: 6.70532e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.11e0

QD
type: SiteQuality
SIO_000300: 1.224e1

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.38e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 337
bin: 8.75e1
variant carriers: 15

GenotypeQuality
all individuals: 333
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1761
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 571
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1163
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 473
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 12

Latino
type: Population
allele count: 1
allele frequency: 1.607717041800643e-3
allele num: 622
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.347826086956522e-4
allele num: 2300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1926
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.221299462628236e-4
allele num: 8188
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.623188405797101e-3
allele num: 276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 55
allele frequency: 5.351235648958941e-3
allele num: 10278
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 5.28e-1

DP
type: SiteQuality
SIO_000300: 5.86665e5

QD
type: SiteQuality
SIO_000300: 1.45e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 7665
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4662
bin: 9.75e1
variant carriers: 82

GenotypeQuality
all individuals: 475
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 302
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 566
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 539
bin: 9.25e1
variant carriers: 10

South Asian
type: Population
allele count: 2
allele frequency: 2.461235540241201e-4
allele num: 8126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 5.443714050944947e-3
allele num: 9736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 6.892895015906681e-3
allele num: 1886
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.633920296570899e-4
allele num: 2158
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.676470588235294e-3
allele num: 272
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.463e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.759999999999999e-2

DP
type: SiteQuality
SIO_000300: 5.73177e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29834
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4590
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 452
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.704164413196323e-4
allele num: 7396
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.67e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.389e0

FS
type: SiteQuality
SIO_000300: 5.37e0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 5.04995e5

QD
type: SiteQuality
SIO_000300: 1.189e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 531
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 6.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.55e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 6.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 4.65763e5

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
all individuals: 1774
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20352
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4562
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.081e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.48e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 4.49467e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 4.074e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

GenotypeQuality
all individuals: 531
bin: 9.25e1
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: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542257865515114e-4
allele num: 6484
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.074e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.225e1

VQSLOD
type: SiteQuality
SIO_000300: -1.081e0

MQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 4.49467e5

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.293326435592343e-4
allele num: 7732
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1132
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6006
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.23582e5

FS
type: SiteQuality
SIO_000300: 1.875e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.252e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.660000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.164e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.744591765526867e-4
allele num: 5732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

DP
type: SiteQuality
SIO_000300: 4.0575e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.64e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.706e0

QD
type: SiteQuality
SIO_000300: 1.309e1

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

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1650
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.541984732824427e-4
allele num: 1048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.495e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.58e-2

DP
type: SiteQuality
SIO_000300: 4.04903e5

FS
type: SiteQuality
SIO_000300: 5.453e0

QD
type: SiteQuality
SIO_000300: 1.43e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.486e0

GenotypeQuality
all individuals: 810
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 984
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.302761855132882e-4
allele num: 7676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.123e0

VQSLOD
type: SiteQuality
SIO_000300: -2.8e0

DP
type: SiteQuality
SIO_000300: 3.93885e5

QD
type: SiteQuality
SIO_000300: 1.362e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 528
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5450
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.955e0

DP
type: SiteQuality
SIO_000300: 3.90222e5

MQRankSum
type: SiteQuality
SIO_000300: -1.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.96e-2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5368
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.176e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: -1.48e0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.95e-2

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.412e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

DP
type: SiteQuality
SIO_000300: 3.82014e5

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 260
bin: 7.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 4.901960784313725e-3
allele num: 204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

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

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.81016e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.325e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.64e-2

GenotypeQuality
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bin: 9.75e1
variant carriers: 33

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 6.152125279642058e-3
allele num: 5364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.807e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.325e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

DP
type: SiteQuality
SIO_000300: 3.81016e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.64e-2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2132
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 1127
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GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.634161114476075e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.198753296571566e-4
allele num: 66736
num of homozygotes: 0

Latino
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East Asian
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European (Finnish)
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African
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Other
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DP
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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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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African
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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QD
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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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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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Other
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South Asian
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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FS
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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Latino
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VQSLOD
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InbreedingCoeff
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DP
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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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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European (Finnish)
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African
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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MQ
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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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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Other
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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FS
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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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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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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VQSLOD
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QD
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FS
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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African
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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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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Other
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num of homozygotes: 0

East Asian
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allele frequency: 7.626531083891842e-3
allele num: 8654
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European (Non-Finnish)
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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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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11578
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Other
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num of homozygotes: 0

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

ReadPosRankSum
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FS
type: SiteQuality
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DP
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
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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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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 5.994305409860632e-5
allele num: 66730
num of homozygotes: 0

East Asian
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Other
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South Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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FS
type: SiteQuality
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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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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Other
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European (Non-Finnish)
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allele frequency: 7.49265719594797e-5
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European (Finnish)
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African
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South Asian
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East Asian
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Latino
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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FS
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MQ
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BaseQRankSum
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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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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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South Asian
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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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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European (Finnish)
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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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African
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South Asian
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DP
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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African
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

Latino
type: Population
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: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

FS
type: SiteQuality
SIO_000300: 6.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.49e-1

DP
type: SiteQuality
SIO_000300: 3.839994e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.217e1

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.736e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeQuality
all individuals: 700
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51844
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 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: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
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: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-1

QD
type: SiteQuality
SIO_000300: 1.162e1

MQRankSum
type: SiteQuality
SIO_000300: -7.89e-1

DP
type: SiteQuality
SIO_000300: 3.839043e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.428e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.067e0

MQ
type: SiteQuality
SIO_000300: 5.926e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 7.75e1
variant carriers: 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: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.837634e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

FS
type: SiteQuality
SIO_000300: 5.575e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.765e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.96e-1

QD
type: SiteQuality
SIO_000300: 1.689e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0