8-124442246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442246
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442246
    reference: chr 8
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.207G>A
  hgvsp: ENST00000523356.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-89G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.178G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.27G>A
  hgvsp: ENST00000523984.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*65G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.189G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.207G>A
  hgvsp: ENST00000522194.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.226G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.207G>A
  hgvsp: ENST00000287387.2:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8509
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala69Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-124442251-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442251
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442251
    reference: chr 8
allele count: 4
allele frequency: 3.29663084327817e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-84C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.183C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.212C>T
  hgvsp: ENSP00000434252.1:p.Pro71Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.212C>T
  hgvsp: ENSP00000428615.1:p.Pro71Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.32C>T
  hgvsp: ENSP00000430427.1:p.Pro11Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*70C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.212C>T
  hgvsp: ENSP00000287387.2:p.Pro71Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.194C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.231C>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro71Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

8-124442260-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442260
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442260
    reference: chr 8
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.41G>T
  hgvsp: ENSP00000430427.1:p.Gly14Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-75G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.221G>T
  hgvsp: ENSP00000428615.1:p.Gly74Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.221G>T
  hgvsp: ENSP00000434252.1:p.Gly74Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.221G>T
  hgvsp: ENSP00000287387.2:p.Gly74Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.240G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.203G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*79G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.192G>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly74Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-124442274-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442274
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442274
    reference: chr 8
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.235G>T
  hgvsp: ENSP00000434252.1:p.Val79Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+1G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+1G>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: c.234+1G>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-124442280-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442280
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442280
    reference: chr 8
allele count: 16
allele frequency: 1.319544097514309e-4
allele num: 121254
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+7C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.241C>G
  hgvsp: ENSP00000434252.1:p.Gln81Glu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+7C>G
  variant of: http://identifiers.org/hgnc/25490
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln81Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

8-124442281-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442281
    reference: chr 8
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.242A>G
  hgvsp: ENSP00000434252.1:p.Gln81Arg
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+8A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+8A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7541
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln81Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

8-124442290-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442290
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442290
    reference: chr 8
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000434252
  ensembl transcript: ENST00000522194
  gene symbol: WDYHV1
  hgvsc: ENST00000522194.1:c.251A>G
  hgvsp: ENSP00000434252.1:p.Gln84Arg
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+17A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+17A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln84Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

8-124442302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442302
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442302
    reference: chr 8
allele count: 11
allele frequency: 9.100084382600639e-5
allele num: 120878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+29C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+29C>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17742
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2491
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

8-124442303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442303
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442303
    reference: chr 8
allele count: 17
allele frequency: 1.406586132715539e-4
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+30G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+30G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20466
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17722
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7549
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-124442305-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442305
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442305
    reference: chr 8
allele count: 2
allele frequency: 1.655656550605143e-5
allele num: 120798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+32A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+32A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8189
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7535
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-124442317-AACCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442317
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442313
    reference: chr 8
allele count: 274
allele frequency: 2.274236387782205e-3
allele num: 120480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+45_54+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+45_*92+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+45_234+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+45_205+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+45_216+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+45_234+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+45_253+48delACCC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+45_-62+48delACCC
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19407
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 4.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15893
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 3.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: AACCC
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

8-124442322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442322
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442322
    reference: chr 8
allele count: 2
allele frequency: 1.670955452327641e-5
allele num: 119692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+49C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+49C>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25689
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7503
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

8-124442327-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442327
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442326
    reference: chr 8
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+55delG
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+55delG
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22491
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: TG
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-124442330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442330
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442330
    reference: chr 8
allele count: 2
allele frequency: 1.665001665001665e-5
allele num: 120120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+57T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+57T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8466
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

8-124442331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442331
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442331
    reference: chr 8
allele count: 1
allele frequency: 8.334444592612349e-6
allele num: 119984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+58C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+58C>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7532
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2719
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22977
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3505
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

8-124442339-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442339
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442339
    reference: chr 8
allele count: 178
allele frequency: 1.485536879704895e-3
allele num: 119822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+66T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+66T>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 13858
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 9988
  bin: 1.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13249
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17306
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 2
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-124442343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124442343
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124442343
    reference: chr 8
allele count: 1
allele frequency: 8.377454594196099e-6
allele num: 119368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.54+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.234+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.234+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.253+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*92+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.216+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.205+70G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-62+70G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15009
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13872
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4322
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2354
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-124448643-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448643
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448643
    reference: chr 8
allele count: 1
allele frequency: 8.677391923083599e-6
allele num: 115242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-50T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-50T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-50T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-50T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-50T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-50T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-807T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-50T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10360
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

8-124448648-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448648
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448648
    reference: chr 8
allele count: 603
allele frequency: 5.230379571160918e-3
allele num: 115288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-45T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-45T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-802T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-45T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-45T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-45T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-45T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-45T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 2.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 3.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 9748
  bin: 1.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 11242
  bin: 1.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.25e1
  variant carriers: 126
genotype quality: GenotypeQuality
  all individuals: 4314
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4867
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 8
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

8-124448650-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448650
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448650
    reference: chr 8
allele count: 1
allele frequency: 8.667013347200554e-6
allele num: 115380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-43A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-800A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-43A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-43A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-43A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-43A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-43A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-43A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12064
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-124448653-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448653
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448653
    reference: chr 8
allele count: 14
allele frequency: 1.212226166767686e-4
allele num: 115490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-40A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-797A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17441
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

8-124448656-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448656
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448656
    reference: chr 8
allele count: 1
allele frequency: 8.654561819535076e-6
allele num: 115546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-794A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-37A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-124448658-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448658
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448658
    reference: chr 8
allele count: 1
allele frequency: 8.649172274213358e-6
allele num: 115618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-35G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-792G>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20680
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3667
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

8-124448662-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448662
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448662
    reference: chr 8
allele count: 2
allele frequency: 1.725714877387958e-5
allele num: 115894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-788C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-31C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-31C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-31C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-31C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-31C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-31C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-31C>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22328
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2985
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20290
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

8-124448663-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448663
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448663
    reference: chr 8
allele count: 69
allele frequency: 5.94509830952422e-4
allele num: 116062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-30T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-30T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-787T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-30T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-30T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-30T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-30T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-30T>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9171
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23051
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5126
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

8-124448666-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448666
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448666
    reference: chr 8
allele count: 12
allele frequency: 1.0323823944389e-4
allele num: 116236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-27G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-784G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-27G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-27G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-27G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-27G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-27G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-27G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24492
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9528
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10443
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

8-124448669-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448669
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448669
    reference: chr 8
allele count: 1
allele frequency: 8.576329331046313e-6
allele num: 116600
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-24A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-24A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-781A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-24A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-24A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-24A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-24A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-24A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25782
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10448
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-124448674-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448674
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448674
    reference: chr 8
allele count: 1
allele frequency: 8.520209937972871e-6
allele num: 117368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-776C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-19C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-19C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-19C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-19C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-19C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-19C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-19C>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

8-124448676-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448676
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448676
    reference: chr 8
allele count: 1
allele frequency: 8.493001766544367e-6
allele num: 117744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-17G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-17G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-17G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-17G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-774G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-17G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-17G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-17G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

8-124448676-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448676
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448676
    reference: chr 8
allele count: 9
allele frequency: 7.64370158988993e-5
allele num: 117744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-17G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-17G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-17G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-17G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-17G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-774G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-17G>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-17G>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28173
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5945
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-124448683-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448683
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448683
    reference: chr 8
allele count: 1
allele frequency: 8.414816809438059e-6
allele num: 118838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-10T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-767T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-10T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-10T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-10T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-10T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-10T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-10T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

8-124448689-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448689
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448689
    reference: chr 8
allele count: 112514
allele frequency: 9.294376156489559e-1
allele num: 121056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.254-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*194-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.235-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.235-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.206-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.55-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.318-4T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-761T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 4.25e1
  variant carriers: 7564
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 8.25e1
  variant carriers: 741
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 3304
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.75e1
  variant carriers: 960
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 8.75e1
  variant carriers: 563
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 4.75e1
  variant carriers: 5887
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 2.75e1
  variant carriers: 5374
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 6.75e1
  variant carriers: 1759
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 3.75e1
  variant carriers: 8214
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 2.25e1
  variant carriers: 2907
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 1100
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 3.25e1
  variant carriers: 7630
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 9.75e1
  variant carriers: 5367
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 5.25e1
  variant carriers: 4436
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 6.25e1
  variant carriers: 2283
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.25e1
  variant carriers: 512
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 7.25e1
  variant carriers: 1293
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.75e1
  variant carriers: 333
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 8.75e1
  variant carriers: 1199
hgvs: c.235-4T>C
num of homozygotes: 52370
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD

8-124448694-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448694
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448694
    reference: chr 8
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.319A>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.56A>T
  hgvsp: ENSP00000430427.1:p.Asp19Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.255A>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.236A>T
  hgvsp: ENSP00000428615.1:p.Asp79Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.236A>T
  hgvsp: ENSP00000287387.2:p.Asp79Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.207A>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-756A>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*195A>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30644
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3336
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp79Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-124448704-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448704
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448704
    reference: chr 8
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*205T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.265T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.66T>G
  hgvsp: ENST00000523984.1:c.66T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.217T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.246T>G
  hgvsp: ENST00000523356.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.329T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-746T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.246T>G
  hgvsp: ENST00000287387.2:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4647
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val82Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS

8-124448715-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448715
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448715
    reference: chr 8
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-735A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.257A>G
  hgvsp: ENSP00000428615.1:p.His86Arg
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.77A>G
  hgvsp: ENSP00000430427.1:p.His26Arg
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.228A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.257A>G
  hgvsp: ENSP00000287387.2:p.His86Arg
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*216A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.340A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.276A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3664
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3361
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His86Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

8-124448718-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448718
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448718
    reference: chr 8
allele count: 5
allele frequency: 4.120177332432388e-5
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.279T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.80T>C
  hgvsp: ENSP00000430427.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.343T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.260T>C
  hgvsp: ENSP00000428615.1:p.Val87Ala
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.260T>C
  hgvsp: ENSP00000287387.2:p.Val87Ala
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.231T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-732T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*219T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30663
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val87Ala
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS

8-124448723-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448723
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448723
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.348A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.284A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.265A>G
  hgvsp: ENSP00000287387.2:p.Ser89Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.85A>G
  hgvsp: ENSP00000430427.1:p.Ser29Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.236A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-727A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.265A>G
  hgvsp: ENSP00000428615.1:p.Ser89Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*224A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9769
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser89Gly
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

8-124448736-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448736
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448736
    reference: chr 8
allele count: 46049
allele frequency: 3.797229322998268e-1
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.278A>G
  hgvsp: ENSP00000287387.2:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*237A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.98A>G
  hgvsp: ENSP00000430427.1:p.Asn33Ser
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.278A>G
  hgvsp: ENSP00000428615.1:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.249A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-714A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.361A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.297A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 9.25e1
  variant carriers: 923
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 4.75e1
  variant carriers: 3300
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 3.75e1
  variant carriers: 1705
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 4.25e1
  variant carriers: 2708
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 5.75e1
  variant carriers: 3814
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 6.75e1
  variant carriers: 3024
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.75e1
  variant carriers: 1937
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 1240
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 9.75e1
  variant carriers: 5753
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 3.25e1
  variant carriers: 1004
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 2.75e1
  variant carriers: 436
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 5.25e1
  variant carriers: 3745
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 6.25e1
  variant carriers: 3425
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 7.25e1
  variant carriers: 2410
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 1521
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 9.25e1
  variant carriers: 140
hgvs: p.Asn93Ser
num of homozygotes: 8918
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

8-124448737-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448737
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448737
    reference: chr 8
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.298C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.279C>G
  hgvsp: ENSP00000287387.2:p.Asn93Lys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.279C>G
  hgvsp: ENSP00000428615.1:p.Asn93Lys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*238C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.362C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.99C>G
  hgvsp: ENSP00000430427.1:p.Asn33Lys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-713C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.250C>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn93Lys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-124448741-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448741
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448741
    reference: chr 8
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.283A>G
  hgvsp: ENSP00000287387.2:p.Ile95Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*242A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.302A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-709A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.366A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.283A>G
  hgvsp: ENSP00000428615.1:p.Ile95Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.103A>G
  hgvsp: ENSP00000430427.1:p.Ile35Val
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.254A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile95Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

8-124448745-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448745
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448745
    reference: chr 8
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.258A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.370A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*246A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-705A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.287A>G
  hgvsp: ENSP00000287387.2:p.Tyr96Cys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.107A>G
  hgvsp: ENSP00000430427.1:p.Tyr36Cys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.287A>G
  hgvsp: ENSP00000428615.1:p.Tyr96Cys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.306A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8030
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr96Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

8-124448746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448746
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448746
    reference: chr 8
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.288T>C
  hgvsp: ENST00000287387.2:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.259T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.288T>C
  hgvsp: ENST00000523356.1:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*247T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-704T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.371T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.108T>C
  hgvsp: ENST00000523984.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.307T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr96Tyr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

8-124448752-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448752
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448752
    reference: chr 8
allele count: 8
allele frequency: 6.589785831960461e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.377C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.114C>T
  hgvsp: ENST00000523984.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.265C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.294C>T
  hgvsp: ENST00000523356.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-698C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.313C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.294C>T
  hgvsp: ENST00000287387.2:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8052
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39828
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3451
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu98Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-124448753-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448753
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448753
    reference: chr 8
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*254G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.378G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.314G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-697G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.295G>A
  hgvsp: ENSP00000287387.2:p.Asp99Asn
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.115G>A
  hgvsp: ENSP00000430427.1:p.Asp39Asn
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.295G>A
  hgvsp: ENSP00000428615.1:p.Asp99Asn
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.266G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp99Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-124448753-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448753
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448753
    reference: chr 8
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.115G>C
  hgvsp: ENSP00000430427.1:p.Asp39His
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.295G>C
  hgvsp: ENSP00000287387.2:p.Asp99His
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.266G>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.295G>C
  hgvsp: ENSP00000428615.1:p.Asp99His
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*254G>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.378G>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-697G>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.314G>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp99His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

8-124448770-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448770
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448769
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.398delC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*274delC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: frameshift_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.315delC
  hgvsp: ENSP00000287387.2:p.Cys106AlafsTer7
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: frameshift_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.315delC
  hgvsp: ENSP00000428615.1:p.Cys106AlafsTer7
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-677delC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.334delC
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: frameshift_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.135delC
  hgvsp: ENSP00000430427.1:p.Cys46AlafsTer7
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.286delC
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys106AlafsTer7
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: TC
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-124448777-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448777
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448776
    reference: chr 8
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.403delT
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.320delT
  hgvsp: ENSP00000287387.2:p.Leu107ProfsTer6
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.140delT
  hgvsp: ENSP00000430427.1:p.Leu47ProfsTer6
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*279delT
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.291delT
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.339delT
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.320delT
  hgvsp: ENSP00000428615.1:p.Leu107ProfsTer6
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-672delT
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu107ProfsTer6
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: CT
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-124448778-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448778
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448778
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.140T>C
  hgvsp: ENSP00000430427.1:p.Leu47Pro
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.320T>C
  hgvsp: ENSP00000428615.1:p.Leu107Pro
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*279T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.320T>C
  hgvsp: ENSP00000287387.2:p.Leu107Pro
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.291T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-672T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.339T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.403T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu107Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

8-124448779-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448779
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448779
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.340C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.321C>G
  hgvsp: ENST00000523356.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-671C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.404C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*280C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.292C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.321C>G
  hgvsp: ENST00000287387.2:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.141C>G
  hgvsp: ENST00000523984.1:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu107Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

8-124448781-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448781
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448781
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*282T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.143T>G
  hgvsp: ENSP00000430427.1:p.Phe48Cys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.294T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.323T>G
  hgvsp: ENSP00000287387.2:p.Phe108Cys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.406T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.342T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.323T>G
  hgvsp: ENSP00000428615.1:p.Phe108Cys
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-669T>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2178
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe108Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

8-124448784-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448784
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448784
    reference: chr 8
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*285A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.345A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.326A>G
  hgvsp: ENSP00000428615.1:p.Asp109Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.146A>G
  hgvsp: ENSP00000430427.1:p.Asp49Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.409A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.326A>G
  hgvsp: ENSP00000287387.2:p.Asp109Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-666A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.297A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp109Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

8-124448791-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448791
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448791
    reference: chr 8
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.333T>C
  hgvsp: ENST00000287387.2:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.153T>C
  hgvsp: ENST00000523984.1:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.333T>C
  hgvsp: ENST00000523356.1:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-659T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.416T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.304T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*292T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.352T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr111Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

8-124448793-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448793
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448793
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.354T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.335T>C
  hgvsp: ENSP00000287387.2:p.Val112Ala
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.306T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.155T>C
  hgvsp: ENSP00000430427.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.335T>C
  hgvsp: ENSP00000428615.1:p.Val112Ala
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-657T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*294T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.418T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val112Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

8-124448800-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448800
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448800
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*301T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.313T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.425T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.342T>A
  hgvsp: ENSP00000428615.1:p.Asp114Glu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-650T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.342T>A
  hgvsp: ENSP00000287387.2:p.Asp114Glu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.162T>A
  hgvsp: ENSP00000430427.1:p.Asp54Glu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.361T>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp114Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-124448802-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448802
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448802
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.363C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-648C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.344C>G
  hgvsp: ENSP00000428615.1:p.Ala115Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.344C>G
  hgvsp: ENSP00000287387.2:p.Ala115Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.427C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.164C>G
  hgvsp: ENSP00000430427.1:p.Ala55Gly
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*303C>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.315C>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala115Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

8-124448804-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448804
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448804
    reference: chr 8
allele count: 46094
allele frequency: 3.797870937973766e-1
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.429T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.317T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.166T>A
  hgvsp: ENSP00000430427.1:p.Phe56Ile
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.346T>A
  hgvsp: ENSP00000428615.1:p.Phe116Ile
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*305T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.346T>A
  hgvsp: ENSP00000287387.2:p.Phe116Ile
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-646T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.365T>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 6.25e1
  variant carriers: 1980
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 9.25e1
  variant carriers: 2569
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 2.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 4.75e1
  variant carriers: 781
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 3.75e1
  variant carriers: 216
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.25e1
  variant carriers: 2600
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 7.75e1
  variant carriers: 2787
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 1132
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.25e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.75e1
  variant carriers: 1514
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 8.25e1
  variant carriers: 2770
genotype depth: GenotypeDepth
  all individuals: 16036
  bin: 9.75e1
  variant carriers: 15084
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 8.75e1
  variant carriers: 2891
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 4.25e1
  variant carriers: 411
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 6.75e1
  variant carriers: 2265
genotype quality: GenotypeQuality
  all individuals: 3153
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Phe116Ile
num of homozygotes: 8940
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-124448806-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448806
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448806
    reference: chr 8
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.319T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-644T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.348T>G
  hgvsp: ENSP00000287387.2:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*307T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.367T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.168T>G
  hgvsp: ENSP00000430427.1:p.Phe56Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.348T>G
  hgvsp: ENSP00000428615.1:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.431T>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe116Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

8-124448824-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448824
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448824
    reference: chr 8
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.366T>G
  hgvsp: ENSP00000428615.1:p.Ile122Met
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.337T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.385T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.449T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*325T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.366T>G
  hgvsp: ENSP00000287387.2:p.Ile122Met
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-626T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.186T>G
  hgvsp: ENSP00000430427.1:p.Ile62Met
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10843
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile122Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

8-124448833-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448833
    reference: chr 8
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.375G>A
  hgvsp: ENST00000523356.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.458G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.394G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*334G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.195G>A
  hgvsp: ENST00000523984.1:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.375G>A
  hgvsp: ENST00000287387.2:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.346G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-617G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9612
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10829
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln125Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

8-124448836-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448836
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448836
    reference: chr 8
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.378T>G
  hgvsp: ENSP00000287387.2:p.Phe126Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.397T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-614T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.198T>G
  hgvsp: ENSP00000430427.1:p.Phe66Leu
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*337T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.461T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.349T>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.378T>G
  hgvsp: ENSP00000428615.1:p.Phe126Leu
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3384
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe126Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

8-124448845-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448845
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448845
    reference: chr 8
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+4A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-605A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+4A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+4A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+4A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+4A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+4A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+4A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10987
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4325
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: c.383+4A>G
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

8-124448847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448847
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448847
    reference: chr 8
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+6G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+6G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+6G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+6G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+6G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-603G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+6G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+6G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.25e1
  variant carriers: 0
hgvs: c.383+6G>A
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-124448850-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448850
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448850
    reference: chr 8
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+9A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-600A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10814
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

8-124448858-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448858
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448858
    reference: chr 8
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+17T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+17T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-592T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+17T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+17T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+17T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+17T>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+17T>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4317
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

8-124448859-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448859
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448859
    reference: chr 8
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+18G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+18G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+18G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+18G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+18G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-591G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+18G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+18G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

8-124448860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448860
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448860
    reference: chr 8
allele count: 3
allele frequency: 2.473288484368817e-5
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+19G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+19G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+19G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+19G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+19G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-590G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+19G>A
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+19G>A
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

8-124448891-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124448891
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124448891
    reference: chr 8
allele count: 2
allele frequency: 1.664031949413429e-5
allele num: 120190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.354+50C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.402+50C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.383+50C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-559C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.203+50C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*342+50C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.466+50C>T
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.383+50C>T
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9925
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10384
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-124449404-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124449404
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124449404
    reference: chr 8
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.384-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*343-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.355-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.403-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.204-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.467-46A>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.384-46A>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7601
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24293
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

8-124449408-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124449408
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124449408
    reference: chr 8
allele count: 2
allele frequency: 1.654779831543413e-5
allele num: 120862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*343-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.355-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.467-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.384-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.403-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.384-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-42A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.204-42A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2670
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5584
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2803
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

8-124449413-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124449413
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124449413
    reference: chr 8
allele count: 4
allele frequency: 3.309012094439205e-5
allele num: 120882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.403-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.384-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.355-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.467-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.384-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*343-37A>G
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.204-37A>G
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9965
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5632
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13877
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum

8-124449416-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124449416
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 124449416
    reference: chr 8
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000517609
  gene symbol: WDYHV1
  hgvsc: ENST00000517609.1:n.467-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000524254
  gene symbol: WDYHV1
  hgvsc: ENST00000524254.1:n.403-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000287387
  ensembl transcript: ENST00000287387
  gene symbol: WDYHV1
  hgvsc: ENST00000287387.2:c.384-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430390
  ensembl transcript: ENST00000519199
  gene symbol: WDYHV1
  hgvsc: ENST00000519199.1:c.*343-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000429258
  ensembl transcript: ENST00000518125
  gene symbol: WDYHV1
  hgvsc: ENST00000518125.1:c.-61-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000428615
  ensembl transcript: ENST00000523356
  gene symbol: WDYHV1
  hgvsc: ENST00000523356.1:c.384-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl protein: ENSP00000430427
  ensembl transcript: ENST00000523984
  gene symbol: WDYHV1
  hgvsc: ENST00000523984.1:c.204-34T>C
  variant of: http://identifiers.org/hgnc/25490
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000156795
  ensembl transcript: ENST00000523551
  gene symbol: WDYHV1
  hgvsc: ENST00000523551.1:n.355-34T>C
  variant of: http://identifiers.org/hgnc/25490
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12708
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

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

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7545
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3799
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32626
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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Latino
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European (Non-Finnish)
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allele frequency: 1.499790029395885e-5
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.999160117583539e-5
allele num: 66676
num of homozygotes: 0

African
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East Asian
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Other
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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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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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

FS
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MQRankSum
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MQ
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SIO_000300: 5.893e1

ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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SIO_000300: -6.826e-1

ReadPosRankSum
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QD
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 15
allele frequency: 9.086503513448025e-4
allele num: 16508
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
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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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66612
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European (Finnish)
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Other
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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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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ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
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DP
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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Latino
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South Asian
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FS
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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European (Non-Finnish)
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Latino
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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MQRankSum
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SIO_000300: 2.36e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

GenotypeQuality
all individuals: 495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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bin: 3.75e1
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GenotypeQuality
all individuals: 2484
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30900
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.01559060341968e-5
allele num: 66322
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: -5.407e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

FS
type: SiteQuality
SIO_000300: 2.253e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.918469e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.15e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

GenotypeQuality
all individuals: 1461
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 272

GenotypeQuality
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GenotypeQuality
all individuals: 2464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.907540220973057e-4
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 224
allele frequency: 3.385629213143496e-3
allele num: 66162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.212488632919066e-3
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.524373259052925e-3
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.494505494505495e-4
allele num: 16380
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.295e1

MQRankSum
type: SiteQuality
SIO_000300: -1.503e0

DP
type: SiteQuality
SIO_000300: 1.893375e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.51e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.477e1

GenotypeQuality
all individuals: 1869
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2674
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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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variant carriers: 0

GenotypeQuality
all individuals: 7486
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variant carriers: 2

GenotypeQuality
all individuals: 1561
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525180733916969e-5
allele num: 65566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.868525e6

VQSLOD
type: SiteQuality
SIO_000300: 4.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.755e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

QD
type: SiteQuality
SIO_000300: 1.443e1

GenotypeQuality
all individuals: 6886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1102
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variant carriers: 0

GenotypeQuality
all individuals: 894
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2552
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2427
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.168e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 6.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.69e-1

MQ
type: SiteQuality
SIO_000300: 5.77e1

DP
type: SiteQuality
SIO_000300: 1.831595e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.544e0

QD
type: SiteQuality
SIO_000300: 1.467e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.1e-1

GenotypeQuality
all individuals: 2718
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22698
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variant carriers: 0

GenotypeQuality
all individuals: 434
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variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2591
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 1382
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variant carriers: 0

GenotypeQuality
all individuals: 2233
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variant carriers: 0

GenotypeQuality
all individuals: 1200
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variant carriers: 0

GenotypeQuality
all individuals: 7535
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variant carriers: 2

GenotypeQuality
all individuals: 6798
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variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032324580023046e-5
allele num: 65956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.603e0

FS
type: SiteQuality
SIO_000300: 6.208e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.826141e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.25e0

QD
type: SiteQuality
SIO_000300: 1.786e1

VQSLOD
type: SiteQuality
SIO_000300: -2.361e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

GenotypeQuality
all individuals: 1211
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2682
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 1200
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variant carriers: 0

GenotypeQuality
all individuals: 2556
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 2413
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variant carriers: 0

GenotypeQuality
all individuals: 557
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variant carriers: 0

GenotypeQuality
all individuals: 253
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variant carriers: 0

GenotypeQuality
all individuals: 1458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.855e1

VQSLOD
type: SiteQuality
SIO_000300: -6.826e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.826212e6

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
all individuals: 2341
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 2466
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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
all individuals: 5988
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2374
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GenotypeQuality
all individuals: 7670
bin: 9.75e1
variant carriers: 174

GenotypeQuality
all individuals: 1053
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.926829268292683e-4
allele num: 10250
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: 147
allele frequency: 2.234993614303959e-3
allele num: 65772
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.2271714922049e-3
allele num: 898
num of homozygotes: 1

Latino
type: Population
allele count: 5
allele frequency: 4.373687893631911e-4
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.165501165501166e-3
allele num: 16302
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.037667071688943e-4
allele num: 6584
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

QD
type: SiteQuality
SIO_000300: 1.555e1

DP
type: SiteQuality
SIO_000300: 1.779682e6

GenotypeQuality
all individuals: 92
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7523
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 620
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GenotypeQuality
all individuals: 5722
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GenotypeQuality
all individuals: 1451
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variant carriers: 0

GenotypeQuality
all individuals: 4601
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variant carriers: 0

GenotypeQuality
all individuals: 2862
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variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.79431929480901e-5
allele num: 10210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.35e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.569e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.185e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 1.766539e6

FS
type: SiteQuality
SIO_000300: 3.203e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.175e0

GenotypeQuality
all individuals: 4637
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5285
bin: 4.75e1
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GenotypeQuality
all individuals: 506
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GenotypeQuality
all individuals: 4247
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GenotypeQuality
all individuals: 190
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GenotypeQuality
all individuals: 2920
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GenotypeQuality
all individuals: 1338
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GenotypeQuality
all individuals: 2657
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GenotypeQuality
all individuals: 7870
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variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5007
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575795776867318e-5
allele num: 63460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

QD
type: SiteQuality
SIO_000300: 8.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.027e0

DP
type: SiteQuality
SIO_000300: 1.821823e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2004
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4175
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2779
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 584
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4765
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2730
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 10780
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10856
bin: 9.75e1
variant carriers: 575

GenotypeQuality
all individuals: 2651
bin: 7.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 435
allele frequency: 6.85060946801474e-3
allele num: 63498
num of homozygotes: 4

African
type: Population
allele count: 5
allele frequency: 4.946576968737634e-4
allele num: 10108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 142
allele frequency: 2.177914110429448e-2
allele num: 6520
num of homozygotes: 4

Latino
type: Population
allele count: 2
allele frequency: 1.804728388377549e-4
allele num: 11082
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.709364908503768e-4
allele num: 14864
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.388888888888889e-2
allele num: 864
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

VQSLOD
type: SiteQuality
SIO_000300: 6.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.836525e6

QD
type: SiteQuality
SIO_000300: 1.484e1

GenotypeQuality
all individuals: 2662
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10393
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4831
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573663173134422e-5
allele num: 63546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.41e-1

QD
type: SiteQuality
SIO_000300: 1.302e1

FS
type: SiteQuality
SIO_000300: 3.061e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.156e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.075e0

DP
type: SiteQuality
SIO_000300: 1.845033e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 2101
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4508
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10410
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 4521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14924
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.263081919884518e-3
allele num: 11084
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.231e0

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

DP
type: SiteQuality
SIO_000300: 1.860895e6

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.717e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

GenotypeQuality
all individuals: 876
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4041
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1945
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2157
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17428
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4662
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.691648822269808e-5
allele num: 14944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11084
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63642
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.878795e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.396e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

VQSLOD
type: SiteQuality
SIO_000300: -3.52e0

QD
type: SiteQuality
SIO_000300: 7.67e0

GenotypeQuality
all individuals: 152
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570302440249992e-5
allele num: 63682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8364
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

DP
type: SiteQuality
SIO_000300: 1.889937e6

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.813e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.782e0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10410
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15042
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.386065378191362e-4
allele num: 8382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.025e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.446e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.914404e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2758
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10470
bin: 9.75e1
variant carriers: 67

GenotypeQuality
all individuals: 1641
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

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

South Asian
type: Population
allele count: 14
allele frequency: 9.275208692195575e-4
allele num: 15094
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.971220185294697e-4
allele num: 10146
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.799532121648371e-4
allele num: 11114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 7.978224141167637e-4
allele num: 63924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

QD
type: SiteQuality
SIO_000300: 1.182e1

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.101e0

DP
type: SiteQuality
SIO_000300: 1.922796e6

GenotypeQuality
all individuals: 1465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22554
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5308
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2827
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

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

African
type: Population
allele count: 10
allele frequency: 9.848335631278313e-4
allele num: 10154
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.796622349982034e-4
allele num: 11132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64014
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.943056e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.441e0

FS
type: SiteQuality
SIO_000300: 9.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
all individuals: 663
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2619
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557680924639397e-5
allele num: 64198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 6.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.961171e6

VQSLOD
type: SiteQuality
SIO_000300: -2.058e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e0

GenotypeQuality
all individuals: 3310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10465
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 1081
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2527
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547939692269589e-5
allele num: 64602
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.604e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

DP
type: SiteQuality
SIO_000300: 1.991862e6

VQSLOD
type: SiteQuality
SIO_000300: 2.35e-1

FS
type: SiteQuality
SIO_000300: 3.014e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.343e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3383
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.529051987767584e-4
allele num: 6540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15592
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
SIO_000300: 2.004494e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

FS
type: SiteQuality
SIO_000300: 3.805e0

QD
type: SiteQuality
SIO_000300: 1.172e1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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variant carriers: 8

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: 2587
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.086896125945362e-5
allele num: 64790
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15592
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.854680767724246e-4
allele num: 10212
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.004494e6

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.172e1

FS
type: SiteQuality
SIO_000300: 3.805e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 621
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530268715186387e-5
allele num: 65348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.052e0

QD
type: SiteQuality
SIO_000300: 2.55e0

DP
type: SiteQuality
SIO_000300: 2.03385e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -3.545e0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 20

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 2468
bin: 9.25e1
variant carriers: 2455

GenotypeQuality
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variant carriers: 713

GenotypeQuality
all individuals: 104
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variant carriers: 103

GenotypeQuality
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variant carriers: 1993

GenotypeQuality
all individuals: 48830
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variant carriers: 48752

GenotypeQuality
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variant carriers: 483

GenotypeQuality
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variant carriers: 289

GenotypeQuality
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variant carriers: 126

GenotypeQuality
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variant carriers: 33

GenotypeQuality
all individuals: 1615
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variant carriers: 1601

GenotypeQuality
all individuals: 1198
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variant carriers: 1153

GenotypeQuality
all individuals: 988
bin: 6.25e1
variant carriers: 817

East Asian
type: Population
allele count: 8604
allele frequency: 9.951422623178349e-1
allele num: 8646
num of homozygotes: 4281

Latino
type: Population
allele count: 10930
allele frequency: 9.484553974314475e-1
allele num: 11524
num of homozygotes: 5190

African
type: Population
allele count: 8763
allele frequency: 8.456861609727852e-1
allele num: 10362
num of homozygotes: 3700

South Asian
type: Population
allele count: 15806
allele frequency: 9.58752881232561e-1
allele num: 16486
num of homozygotes: 7585

European (Finnish)
type: Population
allele count: 6239
allele frequency: 9.458762886597938e-1
allele num: 6596
num of homozygotes: 2951

European (Non-Finnish)
type: Population
allele count: 61326
allele frequency: 9.216965251893712e-1
allele num: 66536
num of homozygotes: 28268

Other
type: Population
allele count: 846
allele frequency: 9.337748344370861e-1
allele num: 906
num of homozygotes: 395

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

FS
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

QD
type: SiteQuality
SIO_000300: 3.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-2

DP
type: SiteQuality
SIO_000300: 3.367237e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

GenotypeQuality
all individuals: 2066
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

QD
type: SiteQuality
SIO_000300: 9.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.971617e6

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

GenotypeQuality
all individuals: 2073
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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
all individuals: 3778
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

DP
type: SiteQuality
SIO_000300: 2.975501e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

QD
type: SiteQuality
SIO_000300: 8.09e0

VQSLOD
type: SiteQuality
SIO_000300: -6.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 85
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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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bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.978514e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.294e1

FS
type: SiteQuality
SIO_000300: 2.844e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

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
all individuals: 3808
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GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995024129972123e-5
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 2.965e1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 2.979186e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

FS
type: SiteQuality
SIO_000300: 1.141e0

GenotypeQuality
all individuals: 4645
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30659
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2316
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3812
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

FS
type: SiteQuality
SIO_000300: 1.159e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.275e0

DP
type: SiteQuality
SIO_000300: 2.98021e6

VQSLOD
type: SiteQuality
SIO_000300: -2.194e0

QD
type: SiteQuality
SIO_000300: 2.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1678
bin: 8.25e1
variant carriers: 88

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 31

GenotypeQuality
all individuals: 2001
bin: 7.75e1
variant carriers: 67

GenotypeQuality
all individuals: 3169
bin: 6.75e1
variant carriers: 47

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 819
bin: 8.75e1
variant carriers: 81

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 42332
bin: 9.75e1
variant carriers: 36481

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 7674
bin: 6.25e1
variant carriers: 42

GenotypeQuality
all individuals: 1300
bin: 7.25e1
variant carriers: 44

African
type: Population
allele count: 3732
allele frequency: 3.587771582388002e-1
allele num: 10402
num of homozygotes: 641

Latino
type: Population
allele count: 4929
allele frequency: 4.265316718587747e-1
allele num: 11556
num of homozygotes: 1027

East Asian
type: Population
allele count: 4806
allele frequency: 5.567655236329935e-1
allele num: 8632
num of homozygotes: 1358

European (Finnish)
type: Population
allele count: 2505
allele frequency: 3.790859564164649e-1
allele num: 6608
num of homozygotes: 488

Other
type: Population
allele count: 329
allele frequency: 3.631346578366446e-1
allele num: 906
num of homozygotes: 59

South Asian
type: Population
allele count: 6724
allele frequency: 4.072683222289522e-1
allele num: 16510
num of homozygotes: 1405

European (Non-Finnish)
type: Population
allele count: 23024
allele frequency: 3.454152664426308e-1
allele num: 66656
num of homozygotes: 3940

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

QD
type: SiteQuality
SIO_000300: 1.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 3.80035e6

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
SIO_000300: 1.145e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

GenotypeQuality
all individuals: 39828
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1527
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.665261e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.914e0

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39828
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

FS
type: SiteQuality
SIO_000300: 8.529e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.04e1

VQSLOD
type: SiteQuality
SIO_000300: -2.306e-1

DP
type: SiteQuality
SIO_000300: 3.665257e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2175
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39827
bin: 9.75e1
variant carriers: 2

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.18e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

FS
type: SiteQuality
SIO_000300: 7.796e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.772e0

DP
type: SiteQuality
SIO_000300: 3.665249e6

QD
type: SiteQuality
SIO_000300: 2.104e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39829
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-1

QD
type: SiteQuality
SIO_000300: 1.59e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

DP
type: SiteQuality
SIO_000300: 3.665261e6

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

QD
type: SiteQuality
SIO_000300: 1.476e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 3.665594e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

GenotypeQuality
all individuals: 2175
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39831
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1524
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.325e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 1.3966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

DP
type: SiteQuality
SIO_000300: 3.66568e6

GenotypeQuality
all individuals: 1524
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3457
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39831
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8055
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.325e1

FS
type: SiteQuality
SIO_000300: 1.3966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

DP
type: SiteQuality
SIO_000300: 3.66568e6

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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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: 2.5e0
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GenotypeQuality
all individuals: 1987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-1

FS
type: SiteQuality
SIO_000300: 5.672e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 3.666011e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 2.683e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.525e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.63e-1

GenotypeQuality
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bin: 6.75e1
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
all individuals: 3
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

FS
type: SiteQuality
SIO_000300: 2.569e0

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

QD
type: SiteQuality
SIO_000300: 1.583e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.408e0

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 6.059e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.666433e6

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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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
all individuals: 8107
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

QD
type: SiteQuality
SIO_000300: 1.395e1

FS
type: SiteQuality
SIO_000300: 8.2e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

DP
type: SiteQuality
SIO_000300: 3.666157e6

MQRankSum
type: SiteQuality
SIO_000300: -7.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 1.459e1

MQRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.666516e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.28e-1

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.84e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

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
all individuals: 1986
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.875e0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.912e1

InbreedingCoeff
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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: 3

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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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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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VQSLOD
type: SiteQuality
SIO_000300: 1.5e-2

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

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
type: Population
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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
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.63e0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

QD
type: SiteQuality
SIO_000300: 1.058e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

DP
type: SiteQuality
SIO_000300: 3.666621e6

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

GenotypeQuality
all individuals: 39835
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.666666e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: 7.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.439e0

FS
type: SiteQuality
SIO_000300: 5.223e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 7771
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variant carriers: 7

GenotypeQuality
all individuals: 745
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1936
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1606
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 1211
bin: 9.25e1
variant carriers: 19

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 8

GenotypeQuality
all individuals: 42916
bin: 9.75e1
variant carriers: 37069

Latino
type: Population
allele count: 4937
allele frequency: 4.265595299809919e-1
allele num: 11574
num of homozygotes: 1031

African
type: Population
allele count: 3734
allele frequency: 3.588314433980396e-1
allele num: 10406
num of homozygotes: 642

East Asian
type: Population
allele count: 4809
allele frequency: 5.567260940032415e-1
allele num: 8638
num of homozygotes: 1359

South Asian
type: Population
allele count: 6724
allele frequency: 4.072683222289522e-1
allele num: 16510
num of homozygotes: 1405

European (Finnish)
type: Population
allele count: 2505
allele frequency: 3.787420622921077e-1
allele num: 6614
num of homozygotes: 488

European (Non-Finnish)
type: Population
allele count: 23055
allele frequency: 3.455589196318835e-1
allele num: 66718
num of homozygotes: 3956

Other
type: Population
allele count: 330
allele frequency: 3.634361233480176e-1
allele num: 908
num of homozygotes: 59

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.755e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

DP
type: SiteQuality
SIO_000300: 4.68503e6

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.497e0

GenotypeQuality
all individuals: 9624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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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GenotypeQuality
all individuals: 10852
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variant carriers: 2

GenotypeQuality
all individuals: 25686
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variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.409e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

DP
type: SiteQuality
SIO_000300: 2.544946e6

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 25683
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4340
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

FS
type: SiteQuality
SIO_000300: 1.819e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.334e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 2.544352e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

GenotypeQuality
all individuals: 3385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

GenotypeQuality
all individuals: 4330
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
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variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25680
bin: 6.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.543185e6

FS
type: SiteQuality
SIO_000300: 3.145e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.188e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.493e1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3122
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variant carriers: 0

GenotypeQuality
all individuals: 1424
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
all individuals: 10828
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variant carriers: 1

GenotypeQuality
all individuals: 25675
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

FS
type: SiteQuality
SIO_000300: 2.393e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.542952e6

QD
type: SiteQuality
SIO_000300: 1.83e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.206e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 25557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10821
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.915e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 1.904e0

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

DP
type: SiteQuality
SIO_000300: 2.540734e6

QD
type: SiteQuality
SIO_000300: 1.267e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10817
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variant carriers: 1

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 25548
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 9575
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.540354e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.333e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.51e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 9561
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 25530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1420
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4319
bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

East Asian
type: Population
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European (Non-Finnish)
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allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

African
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allele frequency: 9.611687812379854e-5
allele num: 10404
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Other
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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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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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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
allele num: 6614
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
allele num: 10404
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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allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.253e0

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

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

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

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

East Asian
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allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.64e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.621e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.994e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.637e0

DP
type: SiteQuality
SIO_000300: 2.532586e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.246882793017456e-4
allele num: 16040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

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

FS
type: SiteQuality
SIO_000300: 3.71e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 1.503216884132043e-5
allele num: 66524
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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 frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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South Asian
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VQSLOD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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FS
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MQRankSum
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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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variant carriers: 2

Latino
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allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66530
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South Asian
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Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.68429207824908e-5
allele num: 10326
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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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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South Asian
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European (Finnish)
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Other
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Latino
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allele num: 11566
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African
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East Asian
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European (Non-Finnish)
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MQRankSum
type: SiteQuality
SIO_000300: 7.03e-1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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DP
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QD
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FS
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ClippingRankSum
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