4-39191401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191401
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191401
    reference: chr 4
allele count: 1
allele frequency: 8.357849692431131e-6
allele num: 119648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224G>A
  hgvsp: ENSP00000425949.1:p.Arg75Lys
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290G>A
  hgvsp: ENSP00000424319.1:p.Arg97Lys
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290G>A
  hgvsp: ENSP00000423706.1:p.Arg97Lys
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113G>A
  hgvsp: ENSP00000426918.1:p.Arg38Lys
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290G>A
  hgvsp: ENSP00000382717.3:p.Arg97Lys
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7218G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290G>A
  hgvsp: ENSP00000423491.1:p.Arg97Lys
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg97Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

4-39191402-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191402
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191402
    reference: chr 4
allele count: 1
allele frequency: 8.358827757995218e-6
allele num: 119634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7219G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+1G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+1G>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
hgvs: c.290+1G>T
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

4-39191428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191428
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191428
    reference: chr 4
allele count: 1
allele frequency: 8.382229673093043e-6
allele num: 119300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7245G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+27G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+27G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41588
  bin: 6.25e1
  variant carriers: 0
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: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

4-39191428-GCTTCACT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191428
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191421
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 119300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+28_290+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+28_290+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+28_113+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+28_290+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+28_-75+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+28_224+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+28_290+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+28_317+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+28_-75+34delCTTCACT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: GCTTCACT
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

4-39191437-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191437
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191436
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 119174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7255delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+37delG
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+37delG
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39264
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5112
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: AG
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/4-39191440-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191440
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191438
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 119162
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+41_290+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+41_290+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+41_-75+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+41_290+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+41_113+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+41_-75+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7259_40+7260delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+41_224+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+41_317+42delCA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+41_290+42delCA
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: AAC
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

4-39191445-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191445
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191445
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 119050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7262G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+44G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+44G>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38852
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/4-39191447-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39191447
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39191447
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 119078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.113+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.317+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.290+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+46A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+7264A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.290+46A>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38731
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS

4-39196114-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196114
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196114
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 45550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-50T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4713T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4713T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-50T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4713T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-50T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-50T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4713T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11931T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4713T>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27527
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14884
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-39196114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196114
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196114
    reference: chr 4
allele count: 1
allele frequency: 2.195389681668496e-5
allele num: 45550
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4713T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4713T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-50T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4713T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4713T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4713T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-50T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11931T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-50T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-50T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13001
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10110
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

4-39196126-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196126
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196126
    reference: chr 4
allele count: 1
allele frequency: 2.156659765355418e-5
allele num: 46368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4725T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-38T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4725T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4725T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4725T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-38T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11943T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-38T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-38T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4725T>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13244
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4188
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/4-39196127-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196127
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196127
    reference: chr 4
allele count: 28
allele frequency: 6.03240261978628e-4
allele num: 46416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4726C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11944C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-37C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-37C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4726C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4726C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4726C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-37C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4726C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-37C>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28424
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8047
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13304
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

4-39196127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196127
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196127
    reference: chr 4
allele count: 472
allele frequency: 1.016890727335402e-2
allele num: 46416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-37C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-37C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-37C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4726C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4726C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4726C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11944C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-37C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4726C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4726C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8047
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 13304
  bin: 1.25e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 1.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 9.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 28424
  bin: 7.5e0
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3522
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5867
  bin: 3.25e1
  variant carriers: 3
num of homozygotes: 4
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

4-39196128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196128
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196128
    reference: chr 4
allele count: 2
allele frequency: 4.258399693395222e-5
allele num: 46966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4727G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4727G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11945G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4727G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-36G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-36G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-36G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-36G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4727G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4727G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13283
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

4-39196133-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196133
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196133
    reference: chr 4
allele count: 2
allele frequency: 4.10391102720893e-5
allele num: 48734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-31T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-31T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11950T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4732T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4732T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4732T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-31T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4732T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4732T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-31T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3822
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5956
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS

4-39196139-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196139
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196139
    reference: chr 4
allele count: 5
allele frequency: 9.968897041231359e-5
allele num: 50156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4738A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4738A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-25A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-25A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4738A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4738A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-25A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-25A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4738A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11956A>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4151
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3739
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

4-39196153-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196153
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196154
    reference: chr 4
allele count: 1
allele frequency: 1.656232402530723e-5
allele num: 60378
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11972dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4754dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-9dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4754dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-9dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-9dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4754dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4754dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-9dupA
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4754dupA
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-39196154-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196154
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196154
    reference: chr 4
allele count: 1
allele frequency: 1.626651050816579e-5
allele num: 61476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4753A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11971A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.318-10A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4753A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4753A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.114-10A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4753A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.291-10A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4753A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.291-10A>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15260
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

4-39196166-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196166
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196166
    reference: chr 4
allele count: 1
allele frequency: 1.259541023251127e-5
allele num: 79394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.320A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4765A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.116A>T
  hgvsp: ENSP00000426918.1:p.Asp39Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4765A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4765A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.293A>T
  hgvsp: ENSP00000423491.1:p.Asp98Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4765A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.293A>T
  hgvsp: ENSP00000382717.3:p.Asp98Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4765A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11983A>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25704
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp98Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-39196170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196170
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196170
    reference: chr 4
allele count: 1
allele frequency: 1.181334908446545e-5
allele num: 84650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.297A>G
  hgvsp: ENST00000506503.1:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.120A>G
  hgvsp: ENST00000509560.1:c.120A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4769A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.297A>G
  hgvsp: ENST00000399820.3:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4769A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.324A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4769A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+11987A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4769A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4769A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln99Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-39196194-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196194
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196194
    reference: chr 4
allele count: 1
allele frequency: 9.735960744606278e-6
allele num: 102712
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.321A>C
  hgvsp: ENSP00000382717.3:p.Lys107Asn
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4793A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.144A>C
  hgvsp: ENSP00000426918.1:p.Lys48Asn
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12011A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.348A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.321A>C
  hgvsp: ENSP00000423491.1:p.Lys107Asn
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4793A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4793A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4793A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4793A>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37756
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys107Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

4-39196199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196199
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196199
    reference: chr 4
allele count: 1
allele frequency: 9.598034322570738e-6
allele num: 104188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4798G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.353G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.149G>A
  hgvsp: ENSP00000426918.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12016G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4798G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.326G>A
  hgvsp: ENSP00000423491.1:p.Gly109Glu
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4798G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.326G>A
  hgvsp: ENSP00000382717.3:p.Gly109Glu
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4798G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4798G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly109Glu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

4-39196200-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196200
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196200
    reference: chr 4
allele count: 1
allele frequency: 9.571026588311863e-6
allele num: 104482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4799A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4799A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12017A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.150A>T
  hgvsp: ENST00000509560.1:c.150A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4799A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.327A>T
  hgvsp: ENST00000399820.3:c.327A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4799A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4799A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.354A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.327A>T
  hgvsp: ENST00000506503.1:c.327A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly109Gly
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-39196206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196206
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196206
    reference: chr 4
allele count: 1
allele frequency: 9.47633758505013e-6
allele num: 105526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4805C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.360C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.333C>T
  hgvsp: ENST00000506503.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4805C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.156C>T
  hgvsp: ENST00000509560.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4805C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4805C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.333C>T
  hgvsp: ENST00000399820.3:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4805C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12023C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe111Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

4-39196216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196216
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196216
    reference: chr 4
allele count: 1
allele frequency: 9.403091736562982e-6
allele num: 106348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4815G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4815G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.166G>A
  hgvsp: ENSP00000426918.1:p.Gly56Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12033G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4815G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.343G>A
  hgvsp: ENSP00000423491.1:p.Gly115Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.343G>A
  hgvsp: ENSP00000382717.3:p.Gly115Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.370G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4815G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4815G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4145
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly115Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-39196220-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196220
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196220
    reference: chr 4
allele count: 1
allele frequency: 9.422939203196261e-6
allele num: 106124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4819C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4819C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4819C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4819C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.170C>A
  hgvsp: ENSP00000426918.1:p.Thr57Asn
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4819C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.374C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.347C>A
  hgvsp: ENSP00000423491.1:p.Thr116Asn
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.347C>A
  hgvsp: ENSP00000382717.3:p.Thr116Asn
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12037C>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr116Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

4-39196248-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196248
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196248
    reference: chr 4
allele count: 1
allele frequency: 1.025788318322631e-5
allele num: 97486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.198T>C
  hgvsp: ENST00000509560.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.375T>C
  hgvsp: ENST00000399820.3:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.402T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.375T>C
  hgvsp: ENST00000506503.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.290+4847T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.224+4847T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4847T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12065T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-75+4847T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-75+4847T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29896
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn125Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

4-39196261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196261
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196261
    reference: chr 4
allele count: 2
allele frequency: 2.183692186749356e-5
allele num: 91588
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.388C>T
  hgvsp: ENSP00000382717.3:p.Arg130Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12078C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4860C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.211C>T
  hgvsp: ENSP00000426918.1:p.Arg71Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4837C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4837C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4837C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.388C>T
  hgvsp: ENSP00000423491.1:p.Arg130Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4837C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.415C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11293
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg130Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ

4-39196262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196262
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196262
    reference: chr 4
allele count: 1
allele frequency: 1.093996149133555e-5
allele num: 91408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4836G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.212G>A
  hgvsp: ENSP00000426918.1:p.Arg71Gln
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4836G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.389G>A
  hgvsp: ENSP00000423491.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.416G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.389G>A
  hgvsp: ENSP00000382717.3:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4861G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12079G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4836G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4836G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg130Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

4-39196278-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196278
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196278
    reference: chr 4
allele count: 2
allele frequency: 2.423185034409228e-5
allele num: 82536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4820T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.405T>C
  hgvsp: ENST00000399820.3:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4820T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.432T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12095T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4877T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4820T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.405T>C
  hgvsp: ENST00000506503.1:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4820T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.228T>C
  hgvsp: ENST00000509560.1:c.228T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16607
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28533
  bin: 2.25e1
  variant carriers: 0
hgvs: c.405T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

4-39196291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196291
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196291
    reference: chr 4
allele count: 2
allele frequency: 2.759153491708744e-5
allele num: 72486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+12C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4807C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12108C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4890C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4807C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4807C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.445C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4807C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+12C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+12C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/4-39196295-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196295
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196295
    reference: chr 4
allele count: 1
allele frequency: 1.448561578352696e-5
allele num: 69034
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+16A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12112A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.449A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+16A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4803A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4803A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4894A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4803A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+16A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4803A>C
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4145
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

4-39196295-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196295
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196295
    reference: chr 4
allele count: 1
allele frequency: 1.448561578352696e-5
allele num: 69034
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+16A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4803A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4803A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4894A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+16A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12112A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+16A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4803A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4803A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.449A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3552
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

4-39196309-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196309
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196309
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 60652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4789A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4789A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4789A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+30A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+30A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+30A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4789A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12126A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.463A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4908A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21463
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3654
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-39196310-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196310
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196310
    reference: chr 4
allele count: 1
allele frequency: 1.685885764380605e-5
allele num: 59316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4788T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+31T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4788T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4909T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.464T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+31T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4788T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12127T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4788T>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+31T>G
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

4-39196317-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196317
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196317
    reference: chr 4
allele count: 1
allele frequency: 1.803491559659501e-5
allele num: 55448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12134T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4781T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+38T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4916T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+38T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4781T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4781T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.471T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4781T>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+38T>A
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9844
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3721
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-39196324-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39196324
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39196324
    reference: chr 4
allele count: 1
allele frequency: 1.944919869301385e-5
allele num: 51416
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.406+45C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+12141C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4774C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.406+45C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000502389
  gene symbol: WDR19
  hgvsc: ENST00000502389.1:n.478C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4774C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4774C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.290+4923C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4774C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.229+45C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5813
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-39201050-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201050
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201050
    reference: chr 4
allele count: 2
allele frequency: 1.99568931108805e-5
allele num: 100216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4212T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-48T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16867T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13252
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7362
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6823
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-39201062-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201062
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201062
    reference: chr 4
allele count: 1
allele frequency: 9.895307645114686e-6
allele num: 101058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4200A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-36A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16879A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6839
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8733
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

4-39201066-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201066
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201066
    reference: chr 4
allele count: 5
allele frequency: 4.910626595953644e-5
allele num: 101820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16883A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-32A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-32A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-32A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4196A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-32A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-32A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-32A>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-32A>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20703
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22714
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6067
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2547
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

4-39201067-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201067
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201065
    reference: chr 4
allele count: 43
allele frequency: 4.213868527301948e-4
allele num: 102044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-30_407-29delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-30_291-29delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-30_407-29delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-30_-74-29delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4194_291-4193delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16885_40+16886delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-30_-74-29delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-30_230-29delAT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-30_225-29delAT
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21821
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: CAT
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

4-39201074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201074
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201074
    reference: chr 4
allele count: 1
allele frequency: 9.520182787509519e-6
allele num: 105040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4188G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-24G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-24G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16891G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-24G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-24G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-24G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-24G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-24G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28317
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7555
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

4-39201076-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201076
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201076
    reference: chr 4
allele count: 1
allele frequency: 9.385969852264834e-6
allele num: 106542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16893A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-22A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4186A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-22A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-22A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-22A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-22A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-22A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-22A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

4-39201089-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201089
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201090
    reference: chr 4
allele count: 1
allele frequency: 8.722045843072952e-6
allele num: 114652
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16911dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-4dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-4dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-4dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-4dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4168dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-4dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-4dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-4dupT
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8526
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

4-39201096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201096
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201096
    reference: chr 4
allele count: 1
allele frequency: 8.493290300662476e-6
allele num: 117740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4166A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-74-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.291-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.407-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.225-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.230-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-74-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16913A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.407-2A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
hgvs: c.407-2A>G
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

4-39201101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201101
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201101
    reference: chr 4
allele count: 5
allele frequency: 4.210880916287688e-5
allele num: 118740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.410A>G
  hgvsp: ENSP00000423491.1:p.Lys137Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.233A>G
  hgvsp: ENSP00000426918.1:p.Lys78Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.4A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.294A>G
  hgvsp: ENST00000506869.1:c.294A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-71A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16918A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.228A>G
  hgvsp: ENST00000505055.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.410A>G
  hgvsp: ENSP00000382717.3:p.Lys137Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-71A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4161A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys137Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

4-39201103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201103
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201103
    reference: chr 4
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.412C>T
  hgvsp: ENSP00000423491.1:p.His138Tyr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4159C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-69C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.235C>T
  hgvsp: ENSP00000426918.1:p.His79Tyr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16920C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.230C>T
  hgvsp: ENSP00000425949.1:p.Thr77Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.412C>T
  hgvsp: ENSP00000382717.3:p.His138Tyr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.296C>T
  hgvsp: ENSP00000424319.1:p.Thr99Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.6C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-69C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3523
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His138Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

4-39201111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201111
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201111
    reference: chr 4
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.420G>A
  hgvsp: ENST00000506503.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-61G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-61G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16928G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.420G>A
  hgvsp: ENST00000399820.3:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.243G>A
  hgvsp: ENST00000509560.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4151G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys140Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

4-39201129-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201129
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201129
    reference: chr 4
allele count: 2
allele frequency: 1.663284654535777e-5
allele num: 120244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-43T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.261T>C
  hgvsp: ENST00000509560.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.438T>C
  hgvsp: ENST00000399820.3:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16946T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4133T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.438T>C
  hgvsp: ENST00000506503.1:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.32T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*19T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*19T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys146Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

4-39201147-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201147
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201147
    reference: chr 4
allele count: 1
allele frequency: 8.311308366163002e-6
allele num: 120318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4115G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16964G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.279G>T
  hgvsp: ENST00000509560.1:c.279G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.456G>T
  hgvsp: ENST00000399820.3:c.456G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.456G>T
  hgvsp: ENST00000506503.1:c.456G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-25G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.50G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-25G>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu152Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

4-39201148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201148
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201148
    reference: chr 4
allele count: 2
allele frequency: 1.662178783950002e-5
allele num: 120324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-24C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.51C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.457C>T
  hgvsp: ENSP00000382717.3:p.Leu153Phe
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-24C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.280C>T
  hgvsp: ENSP00000426918.1:p.Leu94Phe
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.457C>T
  hgvsp: ENSP00000423491.1:p.Leu153Phe
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16965C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4114C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu153Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-39201170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201170
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201170
    reference: chr 4
allele count: 3
allele frequency: 2.498168010125908e-5
allele num: 120088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.479A>G
  hgvsp: ENSP00000423491.1:p.Lys160Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.73A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.479A>G
  hgvsp: ENSP00000382717.3:p.Lys160Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*60A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4092A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*60A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.-2A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.302A>G
  hgvsp: ENSP00000426918.1:p.Lys101Arg
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16987A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys160Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

4-39201181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201181
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201181
    reference: chr 4
allele count: 23
allele frequency: 1.919962602467569e-4
allele num: 119794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.490G>A
  hgvsp: ENSP00000423491.1:p.Val164Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*71G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4081G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*71G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.84G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.313G>A
  hgvsp: ENSP00000426918.1:p.Val105Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.10G>A
  hgvsp: ENSP00000421888.1:p.Val4Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.490G>A
  hgvsp: ENSP00000382717.3:p.Val164Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.10G>A
  hgvsp: ENSP00000288634.7:p.Val4Ile
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+16998G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val164Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

4-39201181-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201181
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201182
    reference: chr 4
allele count: 1
allele frequency: 8.347663488989432e-6
allele num: 119794
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.492dupT
  hgvsp: ENSP00000382717.3:p.Ser165Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.12dupT
  hgvsp: ENSP00000288634.7:p.Ser5Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4079dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.315dupT
  hgvsp: ENSP00000426918.1:p.Ser106Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.492dupT
  hgvsp: ENSP00000423491.1:p.Ser165Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.86dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.12dupT
  hgvsp: ENSP00000421888.1:p.Ser5Ter
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17000dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*73dupT
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*73dupT
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser165Ter
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

4-39201189-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201189
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201189
    reference: chr 4
allele count: 1
allele frequency: 8.376893177858196e-6
allele num: 119376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.321T>C
  hgvsp: ENST00000509560.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.18T>C
  hgvsp: ENST00000288634.7:c.18T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.92T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.498T>C
  hgvsp: ENST00000399820.3:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*79T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*79T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4073T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.498T>C
  hgvsp: ENST00000506503.1:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.18T>C
  hgvsp: ENST00000512112.1:c.18T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17006T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn166Asn
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

4-39201197-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201197
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201197
    reference: chr 4
allele count: 1
allele frequency: 8.429144610404936e-6
allele num: 118636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*87G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.329G>T
  hgvsp: ENSP00000426918.1:p.Gly110Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.26G>T
  hgvsp: ENSP00000288634.7:p.Gly9Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.26G>T
  hgvsp: ENSP00000421888.1:p.Gly9Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.506G>T
  hgvsp: ENSP00000423491.1:p.Gly169Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.506G>T
  hgvsp: ENSP00000382717.3:p.Gly169Val
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17014G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.100G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*87G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4065G>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3897
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly169Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

4-39201203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201203
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201203
    reference: chr 4
allele count: 5
allele frequency: 4.243185444176652e-5
allele num: 117836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4059C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*93C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17020C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.106C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.32C>T
  hgvsp: ENSP00000421888.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.512C>T
  hgvsp: ENSP00000423491.1:p.Thr171Met
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*93C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.512C>T
  hgvsp: ENSP00000382717.3:p.Thr171Met
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.32C>T
  hgvsp: ENSP00000288634.7:p.Thr11Met
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.335C>T
  hgvsp: ENSP00000426918.1:p.Thr112Met
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr171Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

4-39201204-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201204
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201204
    reference: chr 4
allele count: 3
allele frequency: 2.553713098845722e-5
allele num: 117476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.513G>T
  hgvsp: ENST00000506503.1:c.513G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.33G>T
  hgvsp: ENST00000512112.1:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.336G>T
  hgvsp: ENST00000509560.1:c.336G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4058G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17021G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*94G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.513G>T
  hgvsp: ENST00000399820.3:c.513G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.33G>T
  hgvsp: ENST00000288634.7:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*94G>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.107G>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37092
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10263
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr171Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

4-39201209-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201209
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201209
    reference: chr 4
allele count: 1
allele frequency: 8.572506257929568e-6
allele num: 116652
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4053G>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17026G>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.518G>C
  hgvsp: ENSP00000423491.1:p.Arg173Thr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.341G>C
  hgvsp: ENSP00000426918.1:p.Arg114Thr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*99G>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.38G>C
  hgvsp: ENSP00000421888.1:p.Arg13Thr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*99G>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.518G>C
  hgvsp: ENSP00000382717.3:p.Arg173Thr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.38G>C
  hgvsp: ENSP00000288634.7:p.Arg13Thr
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.112G>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg173Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

4-39201219-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201219
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201219
    reference: chr 4
allele count: 2
allele frequency: 1.766004415011038e-5
allele num: 113250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+6A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4043A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17036A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+6A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
hgvs: c.522+6A>G
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-39201222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201222
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201222
    reference: chr 4
allele count: 2
allele frequency: 1.784376003711502e-5
allele num: 112084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4040G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17039G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+9G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+9G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3897
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

4-39201223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201223
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201223
    reference: chr 4
allele count: 2
allele frequency: 1.795719005889958e-5
allele num: 111376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17040T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+10T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4039T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-39201226-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201226
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201226
    reference: chr 4
allele count: 4
allele frequency: 3.621285918629705e-5
allele num: 110458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4036C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17043C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+13C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+13C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

4-39201227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201227
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201227
    reference: chr 4
allele count: 2
allele frequency: 1.830663615560641e-5
allele num: 109250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17044G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4035G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+14G>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+14G>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

4-39201231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201231
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201231
    reference: chr 4
allele count: 1
allele frequency: 9.181218898620981e-6
allele num: 108918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17048C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4031C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+18C>T
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+18C>T
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/4-39201238-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201238
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201238
    reference: chr 4
allele count: 1
allele frequency: 9.360140776517278e-6
allele num: 106836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17055C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4024C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+25C>A
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+25C>A
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14696
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-39201249-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201249
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201249
    reference: chr 4
allele count: 1
allele frequency: 9.706099312808169e-6
allele num: 103028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17066A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4013A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+36A>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+36A>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11084
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

4-39201250-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201250
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201250
    reference: chr 4
allele count: 1
allele frequency: 9.711566475672526e-6
allele num: 102970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17067A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+37A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4012A>G
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+37A>G
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

4-39201254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39201254
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 39201254
    reference: chr 4
allele count: 6
allele frequency: 5.971456438225283e-5
allele num: 100478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000421888
  ensembl transcript: ENST00000512112
  gene symbol: WDR19
  hgvsc: ENST00000512112.1:c.42+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000424319
  ensembl transcript: ENST00000506869
  gene symbol: WDR19
  hgvsc: ENST00000506869.1:c.*103+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423706
  ensembl transcript: ENST00000503697
  gene symbol: WDR19
  hgvsc: ENST00000503697.1:c.291-4008T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000426918
  ensembl transcript: ENST00000509560
  gene symbol: WDR19
  hgvsc: ENST00000509560.1:c.345+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000382717
  ensembl transcript: ENST00000399820
  gene symbol: WDR19
  hgvsc: ENST00000399820.3:c.522+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000425949
  ensembl transcript: ENST00000505055
  gene symbol: WDR19
  hgvsc: ENST00000505055.1:c.*103+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000512448
  gene symbol: WDR19
  hgvsc: ENST00000512448.1:n.116+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl transcript: ENST00000511729
  gene symbol: WDR19
  hgvsc: ENST00000511729.1:n.40+17071T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000288634
  ensembl transcript: ENST00000288634
  gene symbol: WDR19
  hgvsc: ENST00000288634.7:c.42+41T>C
  variant of: http://identifiers.org/hgnc/18340
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157796
  ensembl protein: ENSP00000423491
  ensembl transcript: ENST00000506503
  gene symbol: WDR19
  hgvsc: ENST00000506503.1:c.522+41T>C
  variant of: http://identifiers.org/hgnc/18340
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18157
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12899
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13046
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8063
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 9049
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512081531436175e-5
allele num: 66134
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

DP
type: SiteQuality
SIO_000300: 1.526316e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5442
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 389
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512355948095944e-5
allele num: 66122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.526028e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.629e0

VQSLOD
type: SiteQuality
SIO_000300: 9.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 4.55e0

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

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

GenotypeQuality
all individuals: 1072
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
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: 1
allele frequency: 1.048657718120805e-4
allele num: 9536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.837e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

MQ
type: SiteQuality
SIO_000300: 4.036e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

DP
type: SiteQuality
SIO_000300: 1.504808e6

QD
type: SiteQuality
SIO_000300: 3.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5157
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

MQ
type: SiteQuality
SIO_000300: 4.036e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 1.837e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

DP
type: SiteQuality
SIO_000300: 1.504808e6

QD
type: SiteQuality
SIO_000300: 3.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

GenotypeQuality
all individuals: 39222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 586
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.494849e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.484e0

MQ
type: SiteQuality
SIO_000300: 5.52e1

MQRankSum
type: SiteQuality
SIO_000300: -2.551e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.746e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 5.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.585e-1

GenotypeQuality
all individuals: 453
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38812
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1562
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.492936e6

VQSLOD
type: SiteQuality
SIO_000300: -1.585e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.846e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.793e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.746e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.8e-1

MQ
type: SiteQuality
SIO_000300: 5.52e1

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5073
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1949
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.678e0

VQSLOD
type: SiteQuality
SIO_000300: -3.674e0

MQ
type: SiteQuality
SIO_000300: 5.753e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.552e0

DP
type: SiteQuality
SIO_000300: 1.493829e6

QD
type: SiteQuality
SIO_000300: 2.91e0

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65876
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.495043e6

VQSLOD
type: SiteQuality
SIO_000300: -4.443e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.738e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.738e0

MQ
type: SiteQuality
SIO_000300: 5.816e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 7.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 897
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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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: 9.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4189
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.242e0

DP
type: SiteQuality
SIO_000300: 9.13891e5

MQ
type: SiteQuality
SIO_000300: 5.805e1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

QD
type: SiteQuality
SIO_000300: 4.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 994
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2972
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4932
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.100713524153203e-5
allele num: 24386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3766
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

MQ
type: SiteQuality
SIO_000300: 5.805e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 4.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.242e0

DP
type: SiteQuality
SIO_000300: 9.13891e5

GenotypeQuality
all individuals: 6195
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4815
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 209
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GenotypeQuality
all individuals: 6015
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2984
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.25e1
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GenotypeQuality
all individuals: 240
bin: 7.75e1
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GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.033884630899557e-5
allele num: 24790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3794
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 9.38973e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.187e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.398e0

GenotypeQuality
all individuals: 22754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4717
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3522
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 183
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4589
bin: 9.75e1
variant carriers: 33

GenotypeQuality
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bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 759
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GenotypeQuality
all individuals: 238
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variant carriers: 2

GenotypeQuality
all individuals: 2298
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3816
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 4.436728395061728e-3
allele num: 5184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3770
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.493651979088872e-3
allele num: 2678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.032258064516129e-5
allele num: 24800
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 1.399e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

DP
type: SiteQuality
SIO_000300: 9.4719e5

FS
type: SiteQuality
SIO_000300: 8.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeQuality
all individuals: 771
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6047
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 2857
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4717
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2298
bin: 6.25e1
variant carriers: 15

GenotypeQuality
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GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 10

GenotypeQuality
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bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 441
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3447
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 183
bin: 7.25e1
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GenotypeQuality
all individuals: 214
bin: 8.25e1
variant carriers: 18

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 33

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 26

GenotypeQuality
all individuals: 238
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GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4589
bin: 9.75e1
variant carriers: 493

African
type: Population
allele count: 252
allele frequency: 4.861111111111111e-2
allele num: 5184
num of homozygotes: 3

Latino
type: Population
allele count: 30
allele frequency: 1.120238984316654e-2
allele num: 2678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 3.668763102725367e-3
allele num: 3816
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 1.54639175257732e-2
allele num: 388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 168
allele frequency: 6.774193548387097e-3
allele num: 24800
num of homozygotes: 1

South Asian
type: Population
allele count: 2
allele frequency: 3.460207612456747e-4
allele num: 5780
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 9.4719e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 1.399e1

FS
type: SiteQuality
SIO_000300: 8.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

GenotypeQuality
all individuals: 4782
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 869
bin: 4.25e1
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GenotypeQuality
all individuals: 4145
bin: 9.75e1
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GenotypeQuality
all individuals: 5852
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 213
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GenotypeQuality
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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: 110
bin: 8.75e1
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GenotypeQuality
all individuals: 5998
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.69434090138936e-4
allele num: 5902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.98120869495979e-5
allele num: 25118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2712
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.027e1

MQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 9.47074e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.441e1

GenotypeQuality
all individuals: 200
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
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GenotypeQuality
all individuals: 4861
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GenotypeQuality
all individuals: 562
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variant carriers: 0

GenotypeQuality
all individuals: 2724
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4806
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
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GenotypeQuality
all individuals: 1968
bin: 1.25e1
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GenotypeQuality
all individuals: 217
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 245
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GenotypeQuality
all individuals: 753
bin: 4.25e1
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GenotypeQuality
all individuals: 4147
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variant carriers: 2

GenotypeQuality
all individuals: 26757
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.529084471421346e-4
allele num: 3954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.621796951021732e-4
allele num: 6166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3890
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5366
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.63e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

QD
type: SiteQuality
SIO_000300: 1.332e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

DP
type: SiteQuality
SIO_000300: 9.70875e5

FS
type: SiteQuality
SIO_000300: 1.684e0

GenotypeQuality
all individuals: 295
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3040
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 1.238236750866766e-3
allele num: 4038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.000925e6

QD
type: SiteQuality
SIO_000300: 1.179e1

VQSLOD
type: SiteQuality
SIO_000300: -3.015e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4356
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.240694789081886e-4
allele num: 8060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4860
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.143e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

DP
type: SiteQuality
SIO_000300: 1.126853e6

QD
type: SiteQuality
SIO_000300: 1.024e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.099e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.21921482565228e-4
allele num: 8202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4394
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 9.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.140326e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.452e0

VQSLOD
type: SiteQuality
SIO_000300: -4.036e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5158
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6092
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.421e-1

DP
type: SiteQuality
SIO_000300: 1.308678e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.337e0

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.669e0

FS
type: SiteQuality
SIO_000300: 3.882e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

GenotypeQuality
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7256
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.76731544800982e-5
allele num: 11406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e0

MQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 1.35475e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6034
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.299714062906161e-4
allele num: 7694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56404
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.51697e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6092
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13984
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.746907972887988e-5
allele num: 57244
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.034e1

MQ
type: SiteQuality
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.741492807634705e-5
allele num: 57422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

DP
type: SiteQuality
SIO_000300: 1.53329e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 6.777e0

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4146
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.721466689619556e-5
allele num: 58090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.724e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 7.57e0

DP
type: SiteQuality
SIO_000300: 1.54345e6

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 750
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.707591953826714e-5
allele num: 58562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 1.255e0

QD
type: SiteQuality
SIO_000300: 2.258e1

DP
type: SiteQuality
SIO_000300: 1.552786e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.045e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 40670
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variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.710746912101824e-5
allele num: 58454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7892
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

FS
type: SiteQuality
SIO_000300: 4.328e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

DP
type: SiteQuality
SIO_000300: 1.548936e6

VQSLOD
type: SiteQuality
SIO_000300: -3.27e0

QD
type: SiteQuality
SIO_000300: 1.6e0

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

GenotypeQuality
all individuals: 276
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 3.25e1
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GenotypeQuality
all individuals: 4145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1476
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53306
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.36986301369863e-4
allele num: 7300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.822e0

DP
type: SiteQuality
SIO_000300: 1.427713e6

QD
type: SiteQuality
SIO_000300: 7.41e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.644e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.103e0

GenotypeQuality
all individuals: 4146
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.021879021879022e-5
allele num: 49728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: -8.207e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

QD
type: SiteQuality
SIO_000300: 6.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.95e-1

DP
type: SiteQuality
SIO_000300: 1.34576e6

FS
type: SiteQuality
SIO_000300: 4.301e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2040
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 935
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.707723138584863e-5
allele num: 12974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 7.57e0

VQSLOD
type: SiteQuality
SIO_000300: 9.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.344888e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.45e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.497009488690021e-5
allele num: 44474
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12358
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.32e0

FS
type: SiteQuality
SIO_000300: 6.885e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.779e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

DP
type: SiteQuality
SIO_000300: 1.216874e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 231
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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QD
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MQRankSum
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SIO_000300: 1.16e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 2.018570851836899e-4
allele num: 4954
num of homozygotes: 0

South Asian
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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

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

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

Latino
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South Asian
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allele frequency: 8.86053517632465e-5
allele num: 11286
num of homozygotes: 0

African
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num of homozygotes: 0

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

ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
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num of homozygotes: 0

South Asian
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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
allele num: 5878
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 3536
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African
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South Asian
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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African
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European (Non-Finnish)
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Latino
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MQ
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FS
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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East Asian
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Latino
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African
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South Asian
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VQSLOD
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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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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Latino
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DP
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QD
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6860
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.036307345904869e-5
allele num: 14212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.22811e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.304e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.11e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

GenotypeQuality
all individuals: 1556
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3890
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4328
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6902
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 5.858917272088118e-4
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55890
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.252e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

FS
type: SiteQuality
SIO_000300: 4.151e0

DP
type: SiteQuality
SIO_000300: 1.266743e6

GenotypeQuality
all individuals: 24198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5796
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3976
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3925
bin: 9.75e1
variant carriers: 43

GenotypeQuality
all individuals: 309
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 36
allele frequency: 4.205607476635514e-3
allele num: 8560
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.236245954692557e-4
allele num: 9270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.618122977346278e-4
allele num: 6180
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.993006993006993e-5
allele num: 14300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.569516330537212e-5
allele num: 56030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.771e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 6.049e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.279419e6

VQSLOD
type: SiteQuality
SIO_000300: 5.24e0

GenotypeQuality
all individuals: 3831
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31331
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 208
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.029018316526034e-4
allele num: 9718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57856
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.357168e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.019e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

FS
type: SiteQuality
SIO_000300: 3.802e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33699
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6932
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 542
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3136
bin: 3.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58720
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.133529811834051e-4
allele num: 8822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 1.383467e6

QD
type: SiteQuality
SIO_000300: 1.186e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

GenotypeQuality
all individuals: 292
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 983
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573910853689247e-5
allele num: 63536
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

QD
type: SiteQuality
SIO_000300: 1.407e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: 2.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.668e0

DP
type: SiteQuality
SIO_000300: 1.503265e6

MQ
type: SiteQuality
SIO_000300: 6.148e1

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532895947023116e-5
allele num: 65236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.981e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.808e0

DP
type: SiteQuality
SIO_000300: 1.537675e6

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

QD
type: SiteQuality
SIO_000300: 1.672e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.054e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeQuality
all individuals: 499
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3899
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.893446487505894e-4
allele num: 8484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65766
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16020
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

QD
type: SiteQuality
SIO_000300: 1.534e1

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 3.056e0

DP
type: SiteQuality
SIO_000300: 1.549386e6

GenotypeQuality
all individuals: 3895
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516944267467613e-5
allele num: 65922
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.552785e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.616e0

VQSLOD
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SIO_000300: -2.578e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.147037128104254e-5
allele num: 16268
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 886
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East Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.917e0

MQ
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InbreedingCoeff
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SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.432e0

ReadPosRankSum
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SIO_000300: -2.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

QD
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VQSLOD
type: SiteQuality
SIO_000300: -6.689000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.561214e6

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

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

Latino
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allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503940323647958e-5
allele num: 66492
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 4.264e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
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SIO_000300: 5.963e1

MQRankSum
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SIO_000300: -4.85e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
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SIO_000300: 2.08e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.567748e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.326e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 2.987e0

QD
type: SiteQuality
SIO_000300: 5.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.411e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.569228e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005891547432969e-5
allele num: 66536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.908e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

VQSLOD
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MQRankSum
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SIO_000300: -5.639999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.671e0

DP
type: SiteQuality
SIO_000300: 1.569321e6

QD
type: SiteQuality
SIO_000300: 5.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.516575833308241e-5
allele num: 66422
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8592
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

BaseQRankSum
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QD
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MQRankSum
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SIO_000300: 5.0e-1

FS
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

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

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.168472192884517e-4
allele num: 66278
num of homozygotes: 0

South Asian
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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
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allele num: 6598
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Latino
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allele frequency: 8.722958827634333e-5
allele num: 11464
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Other
type: Population
allele count: 0
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African
type: Population
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allele num: 9760
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MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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type: Population
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allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

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

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16100
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512996641147457e-5
allele num: 66094
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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SIO_000300: 1.334e1

MQRankSum
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SIO_000300: 5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.429999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.55497e6

FS
type: SiteQuality
SIO_000300: 5.737e0

BaseQRankSum
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SIO_000300: 2.18e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.52151421094273e-5
allele num: 65724
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

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

QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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FS
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MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
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allele frequency: 3.561253561253561e-4
allele num: 11232
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.532285250222181e-5
allele num: 65262
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

FS
type: SiteQuality
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QD
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.5331e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.040366208905535e-4
allele num: 9612
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15772
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.073896471166851e-5
allele num: 65064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.52686e6

FS
type: SiteQuality
SIO_000300: 4.805e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

BaseQRankSum
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SIO_000300: -1.704e0

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.548083472660846e-5
allele num: 64596
num of homozygotes: 0

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

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

Other
type: Population
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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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 3.98e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.191421459117891e-5
allele num: 62668
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.199e0

BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
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allele frequency: 1.272912423625254e-4
allele num: 7856
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South Asian
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allele frequency: 6.551362683438155e-5
allele num: 15264
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 7.81e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7792
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.624537006953018e-5
allele num: 61556
num of homozygotes: 0

Other
type: Population
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European (Finnish)
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allele frequency: 1.553760099440646e-4
allele num: 6436
num of homozygotes: 0

DP
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SIO_000300: 1.402488e6

ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.557162060260319e-5
allele num: 61002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.05e0

DP
type: SiteQuality
SIO_000300: 1.374637e6

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 7.42e0

MQ
type: SiteQuality
SIO_000300: 5.818e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.65513110608279e-5
allele num: 15026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.657824933687002e-5
allele num: 60320
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.422e0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

QD
type: SiteQuality
SIO_000300: 1.367e1

VQSLOD
type: SiteQuality
SIO_000300: 9.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.123e0

DP
type: SiteQuality
SIO_000300: 1.340176e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.66306336271412e-5
allele num: 60130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.737e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.3e0

VQSLOD
type: SiteQuality
SIO_000300: -4.779e0

DP
type: SiteQuality
SIO_000300: 1.327329e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 3.677e1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14726
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.357220412595005e-4
allele num: 7368
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.261653e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.057e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.506e-1

QD
type: SiteQuality
SIO_000300: 1.519e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 1.147e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.832e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.758581879572313e-5
allele num: 56864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14320
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.181928e6

FS
type: SiteQuality
SIO_000300: 7.788e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.347e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.972e1

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.983240223463687e-5
allele num: 14320
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.061e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.19e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.625e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.176988e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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