17-1634545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634545
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634545
    reference: chr 17
allele count: 8
allele frequency: 7.053180984624065e-5
allele num: 113424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1536G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.541G>A
  hgvsp: ENSP00000391074.2:p.Val181Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.997G>A
  hgvsp: ENSP00000312074.5:p.Val333Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5340C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4150G>A
  hgvsp: ENSP00000386609.1:p.Val1384Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.469G>A
  hgvsp: ENSP00000407845.1:p.Val157Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1074G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.68G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+306G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.67G>A
  hgvsp: ENSP00000401560.1:p.Val23Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+306G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1074G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17699
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24466
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1384Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/17-1634549-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634549
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634549
    reference: chr 17
allele count: 1
allele frequency: 8.915198630625491e-6
allele num: 112168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.545C>A
  hgvsp: ENSP00000391074.2:p.Thr182Lys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1070C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1070C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+310C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5344G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.71C>A
  hgvsp: ENSP00000401560.1:p.Thr24Lys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4154C>A
  hgvsp: ENSP00000386609.1:p.Thr1385Lys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1001C>A
  hgvsp: ENSP00000312074.5:p.Thr334Lys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.72C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.473C>A
  hgvsp: ENSP00000407845.1:p.Thr158Lys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+310C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1540C>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1385Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

17-1634549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634549
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634549
    reference: chr 17
allele count: 3
allele frequency: 2.674559589187647e-5
allele num: 112168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.545C>T
  hgvsp: ENSP00000391074.2:p.Thr182Met
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1001C>T
  hgvsp: ENSP00000312074.5:p.Thr334Met
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4154C>T
  hgvsp: ENSP00000386609.1:p.Thr1385Met
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.71C>T
  hgvsp: ENSP00000401560.1:p.Thr24Met
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+310C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.72C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.473C>T
  hgvsp: ENSP00000407845.1:p.Thr158Met
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+310C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1070C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1070C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1540C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5344G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23348
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17075
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1385Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

17-1634550-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634550
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634550
    reference: chr 17
allele count: 12
allele frequency: 1.070778455937467e-4
allele num: 112068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1069G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.474G>A
  hgvsp: ENST00000419248.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.73G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4155G>A
  hgvsp: ENST00000409644.1:c.4155G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.72G>A
  hgvsp: ENST00000446363.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5345C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1541G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1069G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1002G>A
  hgvsp: ENST00000309182.5:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.546G>A
  hgvsp: ENST00000437219.2:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+311G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+311G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17221
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4155G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-1634553-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634553
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634553
    reference: chr 17
allele count: 5
allele frequency: 4.51720150332466e-5
allele num: 110688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+314G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+1G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+314G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1066G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1066G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5348C>A
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22133
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4157+1G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-1634561-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634561
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634561
    reference: chr 17
allele count: 1
allele frequency: 9.292298542967588e-6
allele num: 107616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+9C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+9C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+9C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+322C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+9C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+322C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5356G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1058C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1058C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+9C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+9C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+9C>G
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13640
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

17-1634567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634567
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634567
    reference: chr 17
allele count: 1
allele frequency: 9.457337948514252e-6
allele num: 105738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+15C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+15C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+15C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1052C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+15C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+15C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5362G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+328C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1052C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+328C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+15C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+15C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17815
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

17-1634569-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634569
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634569
    reference: chr 17
allele count: 19
allele frequency: 1.815402254920696e-4
allele num: 104660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+330G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+330G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5364C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+17G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1050G>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1050G>C
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16200
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16493
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS

17-1634579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634579
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634579
    reference: chr 17
allele count: 1
allele frequency: 1.001241539508991e-5
allele num: 99876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+340G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5374C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+340G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1040G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+27G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1040G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-1634583-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634583
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634582
    reference: chr 17
allele count: 1
allele frequency: 1.027495787267272e-5
allele num: 97324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+33delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+346delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1034delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+346delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5379delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1034delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+33delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+33delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+33delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+33delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+33delC
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+33delC
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: AC
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-1634586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634586
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634586
    reference: chr 17
allele count: 1
allele frequency: 1.059209829467217e-5
allele num: 94410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+34G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+34G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5381C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+347G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+34G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+34G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1033G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+34G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1033G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+34G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+347G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+34G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

17-1634588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634588
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634588
    reference: chr 17
allele count: 6
allele frequency: 6.461896351182527e-5
allele num: 92852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+349C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1031C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1031C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+36C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+349C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5383G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27471
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

17-1634590-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634590
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634590
    reference: chr 17
allele count: 1
allele frequency: 1.103241323006995e-5
allele num: 90642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+351C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5385G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+351C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1029C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+38C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1029C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26954
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

17-1634593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634593
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634593
    reference: chr 17
allele count: 21
allele frequency: 2.420414467163044e-4
allele num: 86762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+354C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+354C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+41C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1026C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1026C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5388G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25859
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13556
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

17-1634594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634594
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634594
    reference: chr 17
allele count: 4
allele frequency: 4.662874195654201e-5
allele num: 85784
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+355G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1025G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1025G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+42G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+355G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5389C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14137
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25556
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

17-1634604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1634604
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1634604
    reference: chr 17
allele count: 1
allele frequency: 1.327069564986597e-5
allele num: 75354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1543+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1004+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.75+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1015C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.218+365C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4157+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.50+365C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.74+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.548+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.476+52C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.296-5399G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1015C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ

17-1635579-TGCAGAACGGCGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635579
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635567
    reference: chr 17
allele count: 2
allele frequency: 1.674929652954576e-5
allele num: 119408
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14259
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: TGCAGAACGGCGG
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

17-1635584-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635584
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635584
    reference: chr 17
allele count: 1
allele frequency: 8.448943037226043e-6
allele num: 118358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+6001T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-35A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-35A>G
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

17-1635586-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635586
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635586
    reference: chr 17
allele count: 9
allele frequency: 7.607391002992241e-5
allele num: 118306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-33C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5999G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-1635587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635587
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635587
    reference: chr 17
allele count: 2
allele frequency: 1.688362119907478e-5
allele num: 118458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-32G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5998C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

17-1635587-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635587
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635587
    reference: chr 17
allele count: 1
allele frequency: 8.441810599537389e-6
allele num: 118458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5998C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-32G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-32G>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

17-1635589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635589
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635589
    reference: chr 17
allele count: 1
allele frequency: 8.429002511842749e-6
allele num: 118638
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5996G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-30C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-30C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

17-1635590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635590
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635590
    reference: chr 17
allele count: 7
allele frequency: 5.875637926403438e-5
allele num: 119136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5995C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-29G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-29G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

17-1635601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635601
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635601
    reference: chr 17
allele count: 1
allele frequency: 8.365120792344242e-6
allele num: 119544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5984G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-18C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

17-1635602-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635602
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635602
    reference: chr 17
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5983T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-17A>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-17A>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

17-1635614-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635614
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635614
    reference: chr 17
allele count: 34272
allele frequency: 2.853859605296028e-1
allele num: 120090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5971A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-5T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-5T>C
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 2.25e1
  variant carriers: 491
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 280
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 9.25e1
  variant carriers: 1658
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 5.25e1
  variant carriers: 894
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.75e1
  variant carriers: 709
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 9.75e1
  variant carriers: 10813
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 1659
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 7.75e1
  variant carriers: 1599
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 6.25e1
  variant carriers: 1149
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 4.75e1
  variant carriers: 842
genotype depth: GenotypeDepth
  all individuals: 8997
  bin: 3.25e1
  variant carriers: 929
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 6.75e1
  variant carriers: 1381
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 952
genotype quality: GenotypeQuality
hgvs: c.4158-5T>C
num of homozygotes: 5596
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

17-1635618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635618
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635618
    reference: chr 17
allele count: 1
allele frequency: 8.32514693884347e-6
allele num: 120118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5967C>T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544-1G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63-1G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4158-1G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

17-1635619-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635619
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635619
    reference: chr 17
allele count: 1
allele frequency: 8.324176738920521e-6
allele num: 120132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.63G>A
  hgvsp: ENST00000468539.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.477G>A
  hgvsp: ENST00000419248.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.51G>A
  hgvsp: ENSP00000442726.1:p.Trp17Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.76G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.219G>A
  hgvsp: ENSP00000466240.1:p.Val74Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.549G>A
  hgvsp: ENST00000437219.2:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1005G>A
  hgvsp: ENST00000309182.5:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1544G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4158G>A
  hgvsp: ENST00000409644.1:c.4158G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-88G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5966C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.75G>A
  hgvsp: ENST00000446363.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp17Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

17-1635623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635623
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635623
    reference: chr 17
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1548C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1009C>T
  hgvsp: ENSP00000312074.5:p.Pro337Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.481C>T
  hgvsp: ENSP00000407845.1:p.Pro161Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.67C>T
  hgvsp: ENSP00000460742.1:p.Pro23Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-84C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.80C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.79C>T
  hgvsp: ENSP00000401560.1:p.Pro27Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.55C>T
  hgvsp: ENSP00000442726.1:p.Pro19Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.553C>T
  hgvsp: ENSP00000391074.2:p.Pro185Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.223C>T
  hgvsp: ENSP00000466240.1:p.Pro75Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4162C>T
  hgvsp: ENSP00000386609.1:p.Pro1388Ser
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5962G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1388Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

17-1635626-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635626
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635626
    reference: chr 17
allele count: 11
allele frequency: 9.154155986818015e-5
allele num: 120164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1551A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.556A>G
  hgvsp: ENSP00000391074.2:p.Ser186Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1012A>G
  hgvsp: ENSP00000312074.5:p.Ser338Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5959T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.226A>G
  hgvsp: ENSP00000466240.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-81A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.484A>G
  hgvsp: ENSP00000407845.1:p.Ser162Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.70A>G
  hgvsp: ENSP00000460742.1:p.Ser24Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4165A>G
  hgvsp: ENSP00000386609.1:p.Ser1389Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.83A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.58A>G
  hgvsp: ENSP00000442726.1:p.Ser20Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.82A>G
  hgvsp: ENSP00000401560.1:p.Ser28Gly
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Ser1389Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

17-1635633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635633
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635633
    reference: chr 17
allele count: 10
allele frequency: 8.317945134833891e-5
allele num: 120222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.89C>T
  hgvsp: ENSP00000401560.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.90C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1558C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.77C>T
  hgvsp: ENSP00000460742.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-74C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.233C>T
  hgvsp: ENST00000474958.2:c.233C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5952G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.65C>T
  hgvsp: ENSP00000442726.1:p.Ala22Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.491C>T
  hgvsp: ENSP00000407845.1:p.Ala164Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.563C>T
  hgvsp: ENSP00000391074.2:p.Ala188Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4172C>T
  hgvsp: ENSP00000386609.1:p.Ala1391Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1019C>T
  hgvsp: ENSP00000312074.5:p.Ala340Val
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27556
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1391Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

17-1635634-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635634
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635634
    reference: chr 17
allele count: 1
allele frequency: 8.316561600771776e-6
allele num: 120242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.91C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.234C>G
  hgvsp: ENSP00000466240.1:p.Pro79Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4173C>G
  hgvsp: ENST00000409644.1:c.4173C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.66C>G
  hgvsp: ENST00000545662.1:c.66C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.564C>G
  hgvsp: ENST00000437219.2:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.90C>G
  hgvsp: ENST00000446363.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5951G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.492C>G
  hgvsp: ENST00000419248.1:c.492C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1559C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1020C>G
  hgvsp: ENST00000309182.5:c.1020C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-73C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.78C>G
  hgvsp: ENST00000468539.1:c.78C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro79Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-1635635-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635635
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635635
    reference: chr 17
allele count: 1
allele frequency: 8.315178526882972e-6
allele num: 120262
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5950G>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-72C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1560C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.235C>G
  hgvsp: ENSP00000466240.1:p.Pro79Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.493C>G
  hgvsp: ENSP00000407845.1:p.Gln165Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1021C>G
  hgvsp: ENSP00000312074.5:p.Gln341Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.91C>G
  hgvsp: ENSP00000401560.1:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.67C>G
  hgvsp: ENSP00000442726.1:p.Gln23Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4174C>G
  hgvsp: ENSP00000386609.1:p.Gln1392Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.565C>G
  hgvsp: ENSP00000391074.2:p.Gln189Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.92C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.79C>G
  hgvsp: ENSP00000460742.1:p.Gln27Glu
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1392Glu
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: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

17-1635638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635638
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635638
    reference: chr 17
allele count: 2
allele frequency: 1.662399840409615e-5
allele num: 120308
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4177G>A
  hgvsp: ENSP00000386609.1:p.Ala1393Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.496G>A
  hgvsp: ENSP00000407845.1:p.Ala166Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.94G>A
  hgvsp: ENSP00000401560.1:p.Ala32Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1024G>A
  hgvsp: ENSP00000312074.5:p.Ala342Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-69G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.568G>A
  hgvsp: ENSP00000391074.2:p.Ala190Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.95G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.82G>A
  hgvsp: ENSP00000460742.1:p.Ala28Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.238G>A
  hgvsp: ENSP00000466240.1:p.Gly80Asp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.70G>A
  hgvsp: ENSP00000442726.1:p.Ala24Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5947C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1563G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1393Thr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-1635644-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635644
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635644
    reference: chr 17
allele count: 16
allele frequency: 1.328947805574936e-4
allele num: 120396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.574A>G
  hgvsp: ENSP00000391074.2:p.Thr192Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.101A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1569A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.100A>G
  hgvsp: ENSP00000401560.1:p.Thr34Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.244A>G
  hgvsp: ENSP00000466240.1:p.Asp82Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-63A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.502A>G
  hgvsp: ENSP00000407845.1:p.Thr168Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.76A>G
  hgvsp: ENSP00000442726.1:p.Thr26Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.88A>G
  hgvsp: ENSP00000460742.1:p.Thr30Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4183A>G
  hgvsp: ENSP00000386609.1:p.Thr1395Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1030A>G
  hgvsp: ENSP00000312074.5:p.Thr344Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5941T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr1395Ala
num of homozygotes: 1
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-1635646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635646
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635646
    reference: chr 17
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1571C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1032C>T
  hgvsp: ENST00000309182.5:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-61C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.78C>T
  hgvsp: ENST00000545662.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.102C>T
  hgvsp: ENST00000446363.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.576C>T
  hgvsp: ENST00000437219.2:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.90C>T
  hgvsp: ENST00000468539.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4185C>T
  hgvsp: ENST00000409644.1:c.4185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.103C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.246C>T
  hgvsp: ENSP00000466240.1:p.His83Tyr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.504C>T
  hgvsp: ENST00000419248.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5939G>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His83Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

17-1635664-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635664
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635664
    reference: chr 17
allele count: 2
allele frequency: 1.659392994042779e-5
allele num: 120526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.522C>T
  hgvsp: ENST00000419248.1:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.120C>T
  hgvsp: ENST00000446363.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.96C>T
  hgvsp: ENST00000545662.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1050C>T
  hgvsp: ENST00000309182.5:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1589C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4203C>T
  hgvsp: ENST00000409644.1:c.4203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.264C>T
  hgvsp: ENSP00000466240.1:p.His89Tyr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.121C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.108C>T
  hgvsp: ENST00000468539.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.594C>T
  hgvsp: ENST00000437219.2:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5921G>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.His89Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

17-1635667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635667
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635667
    reference: chr 17
allele count: 1
allele frequency: 8.296414289743973e-6
allele num: 120534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5918G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.123C>T
  hgvsp: ENST00000446363.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1053C>T
  hgvsp: ENST00000309182.5:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.525C>T
  hgvsp: ENST00000419248.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1592C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.267C>T
  hgvsp: ENSP00000466240.1:p.Gln90Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.99C>T
  hgvsp: ENST00000545662.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.111C>T
  hgvsp: ENST00000468539.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4206C>T
  hgvsp: ENST00000409644.1:c.4206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.597C>T
  hgvsp: ENST00000437219.2:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.124C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln90Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

17-1635669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635669
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635669
    reference: chr 17
allele count: 93
allele frequency: 7.715281234444998e-4
allele num: 120540
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4208G>A
  hgvsp: ENSP00000386609.1:p.Ser1403Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.101G>A
  hgvsp: ENSP00000442726.1:p.Ser34Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.126G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5916C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.527G>A
  hgvsp: ENSP00000407845.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.599G>A
  hgvsp: ENSP00000391074.2:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.113G>A
  hgvsp: ENSP00000460742.1:p.Ser38Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1055G>A
  hgvsp: ENSP00000312074.5:p.Ser352Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.269G>A
  hgvsp: ENST00000474958.2:c.269G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.125G>A
  hgvsp: ENSP00000401560.1:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-38G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1594G>A
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8869
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 70
genotype quality: GenotypeQuality
hgvs: p.Ser1403Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/17-1635671-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635671
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635671
    reference: chr 17
allele count: 1
allele frequency: 8.296414289743973e-6
allele num: 120534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.601C>A
  hgvsp: ENSP00000391074.2:p.Leu201Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-36C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.271C>A
  hgvsp: ENSP00000466240.1:p.Pro91His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.529C>A
  hgvsp: ENSP00000407845.1:p.Leu177Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4210C>A
  hgvsp: ENSP00000386609.1:p.Leu1404Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.128C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.115C>A
  hgvsp: ENSP00000460742.1:p.Leu39Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1057C>A
  hgvsp: ENSP00000312074.5:p.Leu353Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5914G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.127C>A
  hgvsp: ENSP00000401560.1:p.Leu43Ile
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1596C>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.103C>A
  hgvsp: ENSP00000442726.1:p.Leu35Ile
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1404Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

17-1635676-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635676
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635676
    reference: chr 17
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.606C>T
  hgvsp: ENST00000437219.2:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1601C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1062C>T
  hgvsp: ENST00000309182.5:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.534C>T
  hgvsp: ENST00000419248.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.276C>T
  hgvsp: ENSP00000466240.1:p.Arg93Cys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4215C>T
  hgvsp: ENST00000409644.1:c.4215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.108C>T
  hgvsp: ENST00000545662.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.132C>T
  hgvsp: ENST00000446363.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.120C>T
  hgvsp: ENST00000468539.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.133C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5909G>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg93Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

17-1635677-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635677
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635677
    reference: chr 17
allele count: 3
allele frequency: 2.489006886252385e-5
allele num: 120530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.277G>A
  hgvsp: ENSP00000466240.1:p.Arg93His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.535G>A
  hgvsp: ENSP00000407845.1:p.Ala179Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1063G>A
  hgvsp: ENSP00000312074.5:p.Ala355Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1602G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-30G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.133G>A
  hgvsp: ENSP00000401560.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4216G>A
  hgvsp: ENSP00000386609.1:p.Ala1406Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.109G>A
  hgvsp: ENSP00000442726.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.134G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.121G>A
  hgvsp: ENSP00000460742.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.607G>A
  hgvsp: ENSP00000391074.2:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5908C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala1406Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

17-1635683-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635683
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635683
    reference: chr 17
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4222A>G
  hgvsp: ENSP00000386609.1:p.Ile1408Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.541A>G
  hgvsp: ENSP00000407845.1:p.Ile181Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1069A>G
  hgvsp: ENSP00000312074.5:p.Ile357Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-24A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.127A>G
  hgvsp: ENSP00000460742.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.115A>G
  hgvsp: ENSP00000442726.1:p.Ile39Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1608A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.283A>G
  hgvsp: ENSP00000466240.1:p.His95Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.139A>G
  hgvsp: ENSP00000401560.1:p.Ile47Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5902T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.140A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.613A>G
  hgvsp: ENSP00000391074.2:p.Ile205Val
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1408Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

17-1635686-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635686
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635686
    reference: chr 17
allele count: 34
allele frequency: 2.820921279702642e-4
allele num: 120528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1611T>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1072T>G
  hgvsp: ENSP00000312074.5:p.Cys358Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.130T>G
  hgvsp: ENSP00000460742.1:p.Cys44Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.118T>G
  hgvsp: ENSP00000442726.1:p.Cys40Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.544T>G
  hgvsp: ENSP00000407845.1:p.Cys182Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4225T>G
  hgvsp: ENSP00000386609.1:p.Cys1409Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-21T>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.142T>G
  hgvsp: ENSP00000401560.1:p.Cys48Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.286T>G
  hgvsp: ENSP00000466240.1:p.Leu96Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.616T>G
  hgvsp: ENSP00000391074.2:p.Cys206Gly
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.143T>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5899A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Cys1409Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

17-1635689-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635689
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635689
    reference: chr 17
allele count: 5
allele frequency: 4.148138315523993e-5
allele num: 120536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.133C>T
  hgvsp: ENST00000468539.1:c.133C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.547C>T
  hgvsp: ENST00000419248.1:c.547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.145C>T
  hgvsp: ENST00000446363.1:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1075C>T
  hgvsp: ENST00000309182.5:c.1075C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5896G>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-18C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.289C>T
  hgvsp: ENSP00000466240.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.146C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.121C>T
  hgvsp: ENST00000545662.1:c.121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1614C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4228C>T
  hgvsp: ENST00000409644.1:c.4228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.619C>T
  hgvsp: ENST00000437219.2:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro97Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

17-1635693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635693
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635693
    reference: chr 17
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.293G>A
  hgvsp: ENST00000474958.2:c.293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.551G>A
  hgvsp: ENSP00000407845.1:p.Arg184His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.125G>A
  hgvsp: ENSP00000442726.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.150G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.149G>A
  hgvsp: ENSP00000401560.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4232G>A
  hgvsp: ENSP00000386609.1:p.Arg1411His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1079G>A
  hgvsp: ENSP00000312074.5:p.Arg360His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.137G>A
  hgvsp: ENSP00000460742.1:p.Arg46His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.623G>A
  hgvsp: ENSP00000391074.2:p.Arg208His
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1618G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5892C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1411His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

17-1635695-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635695
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635695
    reference: chr 17
allele count: 2
allele frequency: 1.659310390601666e-5
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.625A>G
  hgvsp: ENSP00000391074.2:p.Ile209Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-12A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.151A>G
  hgvsp: ENSP00000401560.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1620A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.295A>G
  hgvsp: ENSP00000466240.1:p.His99Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.127A>G
  hgvsp: ENSP00000442726.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4234A>G
  hgvsp: ENSP00000386609.1:p.Ile1412Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5890T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.553A>G
  hgvsp: ENSP00000407845.1:p.Ile185Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1081A>G
  hgvsp: ENSP00000312074.5:p.Ile361Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.152A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.139A>G
  hgvsp: ENSP00000460742.1:p.Ile47Val
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1412Val
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

17-1635700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635700
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635700
    reference: chr 17
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.144A>G
  hgvsp: ENST00000468539.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5885T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1625A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.300A>G
  hgvsp: ENSP00000466240.1:p.Thr101Ala
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.630A>G
  hgvsp: ENST00000437219.2:c.630A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1086A>G
  hgvsp: ENST00000309182.5:c.1086A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.156A>G
  hgvsp: ENST00000446363.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.157A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.558A>G
  hgvsp: ENST00000419248.1:c.558A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4239A>G
  hgvsp: ENST00000409644.1:c.4239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.132A>G
  hgvsp: ENST00000545662.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr101Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

17-1635701-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635701
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635701
    reference: chr 17
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.158C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4240C>G
  hgvsp: ENSP00000386609.1:p.Gln1414Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1626C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1087C>G
  hgvsp: ENSP00000312074.5:p.Gln363Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-6C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5884G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.301C>G
  hgvsp: ENSP00000466240.1:p.Thr101Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.631C>G
  hgvsp: ENSP00000391074.2:p.Gln211Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.145C>G
  hgvsp: ENSP00000460742.1:p.Gln49Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.559C>G
  hgvsp: ENSP00000407845.1:p.Gln187Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.133C>G
  hgvsp: ENSP00000442726.1:p.Gln45Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.157C>G
  hgvsp: ENSP00000401560.1:p.Gln53Glu
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1414Glu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

17-1635702-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635702
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635702
    reference: chr 17
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-5A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1627A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.560A>G
  hgvsp: ENSP00000407845.1:p.Gln187Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4241A>G
  hgvsp: ENSP00000386609.1:p.Gln1414Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.134A>G
  hgvsp: ENSP00000442726.1:p.Gln45Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.302A>G
  hgvsp: ENST00000474958.2:c.302A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.146A>G
  hgvsp: ENSP00000460742.1:p.Gln49Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.632A>G
  hgvsp: ENSP00000391074.2:p.Gln211Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1088A>G
  hgvsp: ENSP00000312074.5:p.Gln363Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.158A>G
  hgvsp: ENSP00000401560.1:p.Gln53Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.159A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5883T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1414Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

17-1635703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635703
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635703
    reference: chr 17
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5882C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1089G>A
  hgvsp: ENST00000309182.5:c.1089G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.135G>A
  hgvsp: ENST00000545662.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.633G>A
  hgvsp: ENST00000437219.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.147G>A
  hgvsp: ENST00000468539.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.159G>A
  hgvsp: ENST00000446363.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.561G>A
  hgvsp: ENST00000419248.1:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.160G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.303G>A
  hgvsp: ENSP00000466240.1:p.Gly102Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1628G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4242G>A
  hgvsp: ENST00000409644.1:c.4242G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly102Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

17-1635724-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635724
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635724
    reference: chr 17
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4263G>T
  hgvsp: ENST00000409644.1:c.4263G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1110G>T
  hgvsp: ENST00000309182.5:c.1110G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.156G>T
  hgvsp: ENST00000545662.1:c.156G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.180G>T
  hgvsp: ENST00000446363.1:c.180G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1649G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.18G>T
  hgvsp: ENST00000418841.1:c.18G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.168G>T
  hgvsp: ENST00000468539.1:c.168G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.324G>T
  hgvsp: ENSP00000466240.1:p.Glu109Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5861C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.181G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.582G>T
  hgvsp: ENST00000419248.1:c.582G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.654G>T
  hgvsp: ENST00000437219.2:c.654G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu109Ter
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

17-1635727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635727
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635727
    reference: chr 17
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1113C>T
  hgvsp: ENST00000309182.5:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.327C>T
  hgvsp: ENSP00000466240.1:p.Arg110Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.21C>T
  hgvsp: ENST00000418841.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.183C>T
  hgvsp: ENST00000446363.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.657C>T
  hgvsp: ENST00000437219.2:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.159C>T
  hgvsp: ENST00000545662.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.585C>T
  hgvsp: ENST00000419248.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.171C>T
  hgvsp: ENST00000468539.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4266C>T
  hgvsp: ENST00000409644.1:c.4266C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5858G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.184C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1652C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg110Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-1635732-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635732
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635732
    reference: chr 17
allele count: 1
allele frequency: 8.308546170591069e-6
allele num: 120358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.332C>T
  hgvsp: ENST00000474958.2:c.332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1118C>T
  hgvsp: ENSP00000312074.5:p.Pro373Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.176C>T
  hgvsp: ENSP00000460742.1:p.Pro59Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.26C>T
  hgvsp: ENSP00000395198.1:p.Pro9Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.590C>T
  hgvsp: ENSP00000407845.1:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.189C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4271C>T
  hgvsp: ENSP00000386609.1:p.Pro1424Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.164C>T
  hgvsp: ENSP00000442726.1:p.Pro55Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.188C>T
  hgvsp: ENSP00000401560.1:p.Pro63Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.662C>T
  hgvsp: ENSP00000391074.2:p.Pro221Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1657C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5853G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1424Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

17-1635733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635733
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635733
    reference: chr 17
allele count: 18
allele frequency: 1.495662578522285e-4
allele num: 120348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.27C>T
  hgvsp: ENST00000418841.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4272C>T
  hgvsp: ENST00000409644.1:c.4272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5852G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.165C>T
  hgvsp: ENST00000545662.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.189C>T
  hgvsp: ENST00000446363.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.591C>T
  hgvsp: ENST00000419248.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.190C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1658C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.333C>T
  hgvsp: ENSP00000466240.1:p.Arg112Cys
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.177C>T
  hgvsp: ENST00000468539.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.663C>T
  hgvsp: ENST00000437219.2:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1119C>T
  hgvsp: ENST00000309182.5:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg112Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

17-1635757-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635757
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635757
    reference: chr 17
allele count: 1
allele frequency: 8.338475393159114e-6
allele num: 119926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1143C>G
  hgvsp: ENSP00000312074.5:p.Phe381Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4296C>G
  hgvsp: ENSP00000386609.1:p.Phe1432Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.201C>G
  hgvsp: ENSP00000460742.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.357C>G
  hgvsp: ENSP00000466240.1:p.Leu120Val
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.214C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.51C>G
  hgvsp: ENSP00000395198.1:p.Phe17Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.687C>G
  hgvsp: ENSP00000391074.2:p.Phe229Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.189C>G
  hgvsp: ENSP00000442726.1:p.Phe63Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.615C>G
  hgvsp: ENSP00000407845.1:p.Phe205Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5828G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.213C>G
  hgvsp: ENSP00000401560.1:p.Phe71Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1682C>G
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe1432Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

17-1635757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635757
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635757
    reference: chr 17
allele count: 5
allele frequency: 4.169237696579557e-5
allele num: 119926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.201C>T
  hgvsp: ENST00000468539.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.214C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.687C>T
  hgvsp: ENST00000437219.2:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.189C>T
  hgvsp: ENST00000545662.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5828G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1143C>T
  hgvsp: ENST00000309182.5:c.1143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.615C>T
  hgvsp: ENST00000419248.1:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.213C>T
  hgvsp: ENST00000446363.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.357C>T
  hgvsp: ENSP00000466240.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4296C>T
  hgvsp: ENST00000409644.1:c.4296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.51C>T
  hgvsp: ENST00000418841.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1682C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu120Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

17-1635759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635759
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635759
    reference: chr 17
allele count: 2
allele frequency: 1.668362835549475e-5
allele num: 119878
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4298C>T
  hgvsp: ENSP00000386609.1:p.Ser1433Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.359C>T
  hgvsp: ENST00000474958.2:c.359C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1684C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1145C>T
  hgvsp: ENSP00000312074.5:p.Ser382Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.215C>T
  hgvsp: ENSP00000401560.1:p.Ser72Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.203C>T
  hgvsp: ENSP00000460742.1:p.Ser68Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.216C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.617C>T
  hgvsp: ENSP00000407845.1:p.Ser206Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.191C>T
  hgvsp: ENSP00000442726.1:p.Ser64Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5826G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.689C>T
  hgvsp: ENSP00000391074.2:p.Ser230Phe
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.53C>T
  hgvsp: ENSP00000395198.1:p.Ser18Phe
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1433Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-1635761-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635761
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635761
    reference: chr 17
allele count: 13
allele frequency: 1.085449960756809e-4
allele num: 119766
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5824G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.193C>G
  hgvsp: ENSP00000442726.1:p.Gln65Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.361C>G
  hgvsp: ENSP00000466240.1:p.Ser121Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.218C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.691C>G
  hgvsp: ENSP00000391074.2:p.Gln231Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.205C>G
  hgvsp: ENSP00000460742.1:p.Gln69Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4300C>G
  hgvsp: ENSP00000386609.1:p.Gln1434Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1686C>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.55C>G
  hgvsp: ENSP00000395198.1:p.Gln19Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.619C>G
  hgvsp: ENSP00000407845.1:p.Gln207Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.217C>G
  hgvsp: ENSP00000401560.1:p.Gln73Glu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1147C>G
  hgvsp: ENSP00000312074.5:p.Gln383Glu
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ser121Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

17-1635761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635761
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635761
    reference: chr 17
allele count: 1
allele frequency: 8.349615082744685e-6
allele num: 119766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.193C>T
  hgvsp: ENSP00000442726.1:p.Gln65Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.361C>T
  hgvsp: ENSP00000466240.1:p.Ser121Leu
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.691C>T
  hgvsp: ENSP00000391074.2:p.Gln231Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.217C>T
  hgvsp: ENSP00000401560.1:p.Gln73Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.619C>T
  hgvsp: ENSP00000407845.1:p.Gln207Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.55C>T
  hgvsp: ENSP00000395198.1:p.Gln19Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4300C>T
  hgvsp: ENSP00000386609.1:p.Gln1434Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.218C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5824G>A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.205C>T
  hgvsp: ENSP00000460742.1:p.Gln69Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1147C>T
  hgvsp: ENSP00000312074.5:p.Gln383Ter
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1686C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1434Ter
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

17-1635762-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635762
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635762
    reference: chr 17
allele count: 3
allele frequency: 2.507606406098499e-5
allele num: 119636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.218A>G
  hgvsp: ENSP00000401560.1:p.Gln73Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.362A>G
  hgvsp: ENST00000474958.2:c.362A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.219A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.206A>G
  hgvsp: ENSP00000460742.1:p.Gln69Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1687A>G
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4301A>G
  hgvsp: ENSP00000386609.1:p.Gln1434Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.620A>G
  hgvsp: ENSP00000407845.1:p.Gln207Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.692A>G
  hgvsp: ENSP00000391074.2:p.Gln231Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5823T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1148A>G
  hgvsp: ENSP00000312074.5:p.Gln383Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.56A>G
  hgvsp: ENSP00000395198.1:p.Gln19Arg
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.194A>G
  hgvsp: ENSP00000442726.1:p.Gln65Arg
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1434Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

17-1635766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635766
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635766
    reference: chr 17
allele count: 1
allele frequency: 8.364001338240215e-6
allele num: 119560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.60G>A
  hgvsp: ENST00000418841.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5819C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.624G>A
  hgvsp: ENST00000419248.1:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1152G>A
  hgvsp: ENST00000309182.5:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.696G>A
  hgvsp: ENST00000437219.2:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.222G>A
  hgvsp: ENST00000446363.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.198G>A
  hgvsp: ENST00000545662.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.223G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4305G>A
  hgvsp: ENST00000409644.1:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1691G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.366G>A
  hgvsp: ENSP00000466240.1:p.Ala123Thr
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.210G>A
  hgvsp: ENST00000468539.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26600
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala123Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

17-1635774-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635774
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635774
    reference: chr 17
allele count: 1
allele frequency: 8.39545973537511e-6
allele num: 119112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1160T>C
  hgvsp: ENSP00000312074.5:p.Leu387Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.218T>C
  hgvsp: ENSP00000460742.1:p.Leu73Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5811A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.68T>C
  hgvsp: ENSP00000395198.1:p.Leu23Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.704T>C
  hgvsp: ENSP00000391074.2:p.Leu235Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.231T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4313T>C
  hgvsp: ENSP00000386609.1:p.Leu1438Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.*3T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.632T>C
  hgvsp: ENSP00000407845.1:p.Leu211Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.206T>C
  hgvsp: ENSP00000442726.1:p.Leu69Pro
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1699T>C
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.230T>C
  hgvsp: ENSP00000401560.1:p.Leu77Pro
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1438Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

17-1635776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635776
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635776
    reference: chr 17
allele count: 9
allele frequency: 7.56442367496512e-5
allele num: 118978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.*5C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.634C>T
  hgvsp: ENSP00000407845.1:p.Arg212Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.220C>T
  hgvsp: ENSP00000460742.1:p.Arg74Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4315C>T
  hgvsp: ENSP00000386609.1:p.Arg1439Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.232C>T
  hgvsp: ENSP00000401560.1:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.208C>T
  hgvsp: ENSP00000442726.1:p.Arg70Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.706C>T
  hgvsp: ENSP00000391074.2:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5809G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1162C>T
  hgvsp: ENSP00000312074.5:p.Arg388Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.70C>T
  hgvsp: ENSP00000395198.1:p.Arg24Trp
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1701C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.233C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8610
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15301
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg1439Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

17-1635777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635777
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635777
    reference: chr 17
allele count: 5
allele frequency: 4.208825064395024e-5
allele num: 118798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.209G>A
  hgvsp: ENSP00000442726.1:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1702G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4316G>A
  hgvsp: ENSP00000386609.1:p.Arg1439Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.*6G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5808C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.635G>A
  hgvsp: ENSP00000407845.1:p.Arg212Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1163G>A
  hgvsp: ENSP00000312074.5:p.Arg388Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.234G>A
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.221G>A
  hgvsp: ENSP00000460742.1:p.Arg74Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.707G>A
  hgvsp: ENSP00000391074.2:p.Arg236Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.71G>A
  hgvsp: ENSP00000395198.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.233G>A
  hgvsp: ENSP00000401560.1:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25749
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15051
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg1439Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

17-1635788-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635788
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635788
    reference: chr 17
allele count: 1
allele frequency: 8.475294516484449e-6
allele num: 117990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.714+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4323+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.240+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.642+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.241+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1709+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.78+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.228+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1170+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.*13+4G>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5797C>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.216+4G>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14085
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4323+4G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

17-1635803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1635803
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1635803
    reference: chr 17
allele count: 3
allele frequency: 2.601817803371956e-5
allele num: 115304
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000386609
  ensembl transcript: ENST00000409644
  gene symbol: WDR81
  hgvsc: ENST00000409644.1:c.4323+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000391074
  ensembl transcript: ENST00000437219
  gene symbol: WDR81
  hgvsc: ENST00000437219.2:c.714+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000401560
  ensembl transcript: ENST00000446363
  gene symbol: WDR81
  hgvsc: ENST00000446363.1:c.240+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000464528
  gene symbol: WDR81
  hgvsc: ENST00000464528.1:n.1709+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000466240
  ensembl transcript: ENST00000474958
  gene symbol: WDR81
  hgvsc: ENST00000474958.2:c.*13+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000407845
  ensembl transcript: ENST00000419248
  gene symbol: WDR81
  hgvsc: ENST00000419248.1:c.642+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl transcript: ENST00000495411
  gene symbol: WDR81
  hgvsc: ENST00000495411.1:n.241+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000312074
  ensembl transcript: ENST00000309182
  gene symbol: WDR81
  hgvsc: ENST00000309182.5:c.1170+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262791
  ensembl transcript: ENST00000576540
  gene symbol: RP11-961A15.1
  hgvsc: ENST00000576540.1:n.295+5782G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000395198
  ensembl transcript: ENST00000418841
  gene symbol: WDR81
  hgvsc: ENST00000418841.1:c.78+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000442726
  ensembl transcript: ENST00000545662
  gene symbol: WDR81
  hgvsc: ENST00000545662.1:c.216+19C>T
  variant of: http://identifiers.org/hgnc/26600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167716
  ensembl protein: ENSP00000460742
  ensembl transcript: ENST00000468539
  gene symbol: WDR81
  hgvsc: ENST00000468539.1:c.228+19C>T
  variant of: http://identifiers.org/hgnc/26600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11062
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 404
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5382
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 39389
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598414372942042e-5
allele num: 62562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

Latino
type: Population
allele count: 7
allele frequency: 6.311992786293959e-4
allele num: 11090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15074
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

FS
type: SiteQuality
SIO_000300: 4.261e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.903e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 1.41382e6

GenotypeDepth
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 715
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.61363196282192e-5
allele num: 61972
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.121e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

DP
type: SiteQuality
SIO_000300: 1.383308e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

GenotypeDepth
all individuals: 15
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14804
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.227263925643839e-5
allele num: 61972
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.222493887530562e-4
allele num: 8180
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.121e1

FS
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.383308e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

GenotypeDepth
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23306
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5110
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8539
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5814
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.420138162026376e-4
allele num: 9554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14810
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.110787172011662e-5
allele num: 10976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.229765519023319e-5
allele num: 61924
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: 8.500000000000001e-2

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61230
num of homozygotes: 0

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: 0.0e0
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num of homozygotes: 0

Other
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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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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 8.719916288803627e-4
allele num: 5734
num of homozygotes: 0

FS
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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allele frequency: 1.278772378516624e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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MQRankSum
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FS
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -2.0e-3

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5430
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 58702
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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BaseQRankSum
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FS
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QD
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VQSLOD
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SIO_000300: 8.699999999999999e-2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

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

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

Latino
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African
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allele frequency: 1.996893720878633e-3
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 1.333333333333333e-3
allele num: 750
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 55648
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.189909566872918e-4
allele num: 8404
num of homozygotes: 0

Other
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

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

South Asian
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Latino
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European (Finnish)
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African
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
type: SiteQuality
SIO_000300: 3.03e0

GenotypeDepth
all individuals: 3687
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8562
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6705
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4471
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8974
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.477567298105683e-4
allele num: 8024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51964
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.11e1

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

DP
type: SiteQuality
SIO_000300: 8.34515e5

FS
type: SiteQuality
SIO_000300: 4.133e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.177e0

GenotypeDepth
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8836
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23305
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4853
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3070
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6784
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1059
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.823010411152286e-5
allele num: 11334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

DP
type: SiteQuality
SIO_000300: 8.111e5

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2649
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 7.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3496
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 662
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3862
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21662
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2216
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1516
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6763
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8909
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.048592616872209e-5
allele num: 48814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.850823616509347e-3
allele num: 10806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4374
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 6.263e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 7.85535e5

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6779
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5207
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3604
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 555
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8924
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 655
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.316191540898081e-5
allele num: 10734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.0290088638195e-4
allele num: 7446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48274
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

FS
type: SiteQuality
SIO_000300: 2.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 7.77476e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.567e1

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3782
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8813
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.331872026863166e-5
allele num: 42884
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.48039e5

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.151e0

QD
type: SiteQuality
SIO_000300: 1.524e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
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variant carriers: 0

GenotypeQuality
all individuals: 423
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7148
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23587
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 883
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.217433649866082e-4
allele num: 16428
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.513e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.356e0

DP
type: SiteQuality
SIO_000300: 2.524677e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.97e-1

FS
type: SiteQuality
SIO_000300: 7.191e0

MQ
type: SiteQuality
SIO_000300: 4.993e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

QD
type: SiteQuality
SIO_000300: 5.12e0

GenotypeDepth
all individuals: 9239
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
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variant carriers: 0

GenotypeQuality
all individuals: 2337
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variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 16889
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 6738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22245
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 276
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.886e0

VQSLOD
type: SiteQuality
SIO_000300: -2.566e0

FS
type: SiteQuality
SIO_000300: 6.303e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e0

DP
type: SiteQuality
SIO_000300: 2.508339e6

MQRankSum
type: SiteQuality
SIO_000300: -1.356e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.139e1

GenotypeDepth
all individuals: 1429
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22243
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
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GenotypeQuality
all individuals: 6707
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variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16890
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 3
allele frequency: 2.598302442404296e-4
allele num: 11546
num of homozygotes: 0

South Asian
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allele count: 6
allele frequency: 3.659875564230816e-4
allele num: 16394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64564
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -3.7e-1

VQSLOD
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QD
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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DP
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SIO_000300: 2.506355e6

ClippingRankSum
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SIO_000300: -1.327e0

InbreedingCoeff
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SIO_000300: -5.0e-4

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
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allele frequency: 2.038735983690112e-4
allele num: 9810
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64652
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.273e0

QD
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SIO_000300: 1.368e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

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

East Asian
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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DP
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.894e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.544783266907653e-5
allele num: 64734
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQ
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QD
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DP
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SIO_000300: 2.485263e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 2.992817238627295e-4
allele num: 10024
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.537846399901578e-5
allele num: 65026
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
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allele frequency: 1.732501732501733e-4
allele num: 11544
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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FS
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DP
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.531252871099133e-5
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num of homozygotes: 0

African
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South Asian
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East Asian
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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FS
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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European (Non-Finnish)
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Latino
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East Asian
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QD
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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variant carriers: 910

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 440
bin: 8.75e1
variant carriers: 66

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 41

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 23

African
type: Population
allele count: 645
allele frequency: 6.326010200078462e-2
allele num: 10196
num of homozygotes: 28

Latino
type: Population
allele count: 2074
allele frequency: 1.794738663897542e-1
allele num: 11556
num of homozygotes: 216

European (Finnish)
type: Population
allele count: 2210
allele frequency: 3.344430992736078e-1
allele num: 6608
num of homozygotes: 386

European (Non-Finnish)
type: Population
allele count: 20339
allele frequency: 3.093195851202969e-1
allele num: 65754
num of homozygotes: 3224

East Asian
type: Population
allele count: 4375
allele frequency: 5.076583894174983e-1
allele num: 8618
num of homozygotes: 1082

Other
type: Population
allele count: 264
allele frequency: 2.946428571428572e-1
allele num: 896
num of homozygotes: 44

South Asian
type: Population
allele count: 4365
allele frequency: 2.651561171182116e-1
allele num: 16462
num of homozygotes: 616

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 1.655e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

FS
type: SiteQuality
SIO_000300: 1.253e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

DP
type: SiteQuality
SIO_000300: 3.339041e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.49e-2

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

GenotypeDepth
all individuals: 69
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1932
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12269
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 565
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 733
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 3887
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variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3925
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.904e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 2.892e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.847e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.76207e6

GenotypeDepth
all individuals: 500
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
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variant carriers: 0

GenotypeDepth
all individuals: 528
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variant carriers: 0

GenotypeDepth
all individuals: 8598
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variant carriers: 0

GenotypeQuality
all individuals: 563
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 2023
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variant carriers: 1

GenotypeQuality
all individuals: 60
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variant carriers: 0

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

GenotypeQuality
all individuals: 3921
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variant carriers: 0

GenotypeQuality
all individuals: 1933
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

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

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
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variant carriers: 0

GenotypeQuality
all individuals: 33762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12263
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variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 4.969e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 1.762389e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.096e0

QD
type: SiteQuality
SIO_000300: 9.74e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: -7.274e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.984e0

GenotypeDepth
all individuals: 4277
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 12269
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variant carriers: 0

GenotypeQuality
all individuals: 730
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variant carriers: 0

GenotypeQuality
all individuals: 536
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variant carriers: 0

GenotypeQuality
all individuals: 3923
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 745
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variant carriers: 0

GenotypeQuality
all individuals: 33803
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variant carriers: 0

GenotypeQuality
all individuals: 1934
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variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
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: 65710
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

FS
type: SiteQuality
SIO_000300: 4.155e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.08e-1

QD
type: SiteQuality
SIO_000300: 9.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.265e0

DP
type: SiteQuality
SIO_000300: 1.763235e6

GenotypeDepth
all individuals: 16420
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 1925
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33882
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 726
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3877
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variant carriers: 0

GenotypeQuality
all individuals: 12281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 744
bin: 9.25e1
variant carriers: 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: 8
allele frequency: 1.217174329793385e-4
allele num: 65726
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.950458357714063e-4
allele num: 10254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.263e1

DP
type: SiteQuality
SIO_000300: 1.764193e6

GenotypeDepth
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
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variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 746
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variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 3873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
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variant carriers: 10

GenotypeQuality
all individuals: 12280
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GenotypeQuality
all individuals: 723
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GenotypeQuality
all individuals: 46
bin: 4.25e1
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GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 2.25e1
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GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 34053
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GenotypeQuality
all individuals: 3911
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variant carriers: 0

GenotypeQuality
all individuals: 1920
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variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65754
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: 8628
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.455868089233754e-4
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.578e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.959e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

QD
type: SiteQuality
SIO_000300: 1.854e1

DP
type: SiteQuality
SIO_000300: 1.765038e6

VQSLOD
type: SiteQuality
SIO_000300: -9.959e-1

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 25
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variant carriers: 0

GenotypeDepth
all individuals: 76
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GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 12295
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GenotypeQuality
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GenotypeQuality
all individuals: 723
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 1976
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GenotypeQuality
all individuals: 474
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 3916
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 1921
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GenotypeQuality
all individuals: 55
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 51
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GenotypeQuality
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GenotypeQuality
all individuals: 3878
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GenotypeQuality
all individuals: 81
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
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: 894
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.764676e6

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.913e1

MQRankSum
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SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

FS
type: SiteQuality
SIO_000300: 4.815e0

QD
type: SiteQuality
SIO_000300: 7.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.753e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.471e0

GenotypeDepth
all individuals: 137
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
all individuals: 65
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GenotypeQuality
all individuals: 3916
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GenotypeQuality
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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: 100
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GenotypeQuality
all individuals: 109
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GenotypeQuality
all individuals: 1973
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variant carriers: 1

GenotypeQuality
all individuals: 34130
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GenotypeQuality
all individuals: 472
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.520218911523259e-5
allele num: 65780
num of homozygotes: 0

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

South Asian
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ReadPosRankSum
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SIO_000300: 7.51e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

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

Other
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num of homozygotes: 0

South Asian
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allele frequency: 1.21153380179307e-4
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65820
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -1.72e-1

VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele num: 65882
num of homozygotes: 0

European (Finnish)
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allele num: 6614
num of homozygotes: 1

African
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Other
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MQRankSum
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SIO_000300: 8.500000000000001e-2

FS
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MQ
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SIO_000300: 5.921e1

ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 65920
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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South Asian
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allele num: 16508
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European (Finnish)
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num of homozygotes: 0

Other
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DP
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SIO_000300: 1.767447e6

ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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MQ
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SIO_000300: 5.928e1

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
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allele num: 65990
num of homozygotes: 0

East Asian
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African
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European (Finnish)
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num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

East Asian
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Other
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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DP
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QD
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ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele num: 66000
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East Asian
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African
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South Asian
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InbreedingCoeff
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QD
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515289268721399e-5
allele num: 65994
num of homozygotes: 0

Other
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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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VQSLOD
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -4.0e-4

BaseQRankSum
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SIO_000300: -3.248e0

FS
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MQRankSum
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SIO_000300: 7.19e-1

MQ
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ClippingRankSum
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DP
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SIO_000300: 1.765675e6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11562
num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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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: 10330
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 8.1e-2

MQRankSum
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DP
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SIO_000300: 1.765894e6

FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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SIO_000300: 7.82e-1

VQSLOD
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MQ
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SIO_000300: 5.925e1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

South Asian
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allele count: 0
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European (Non-Finnish)
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allele num: 65992
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Other
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Latino
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European (Finnish)
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num of homozygotes: 0

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

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

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

Latino
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allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

European (Finnish)
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allele count: 0
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African
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East Asian
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Other
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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QD
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
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num of homozygotes: 0

Other
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European (Finnish)
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allele num: 6614
num of homozygotes: 0

African
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allele num: 10330
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South Asian
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European (Non-Finnish)
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allele frequency: 4.394871639438669e-4
allele num: 65986
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 65996
num of homozygotes: 0

European (Finnish)
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East Asian
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African
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South Asian
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Other
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Latino
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele num: 65834
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African
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Latino
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Other
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South Asian
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European (Finnish)
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FS
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DP
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 7.626136294307851e-5
allele num: 65564
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East Asian
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South Asian
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European (Finnish)
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Other
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African
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Latino
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DP
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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Latino
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African
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South Asian
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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South Asian
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East Asian
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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African
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Latino
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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QD
type: SiteQuality
SIO_000300: 1.737e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.827262760384943e-4
allele num: 16418
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.348e0

MQRankSum
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SIO_000300: 3.52e-1

VQSLOD
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ClippingRankSum
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.735818e6

BaseQRankSum
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SIO_000300: 5.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.695e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65386
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.788566953797964e-5
allele num: 10216
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

QD
type: SiteQuality
SIO_000300: 6.16e0

DP
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SIO_000300: 1.731279e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 2.22e-1

VQSLOD
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SIO_000300: -2.872e0

MQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.831e1

GenotypeDepth
all individuals: 48
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 11797
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.852216748768474e-5
allele num: 10150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65176
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.55e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
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SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 1.029e0

QD
type: SiteQuality
SIO_000300: 1.231e1

ReadPosRankSum
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SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: 9.58e-1

DP
type: SiteQuality
SIO_000300: 1.7042e6

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1718
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.228765397966393e-4
allele num: 65106
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.696264e6

FS
type: SiteQuality
SIO_000300: 2.063e0

MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.22e-1

QD
type: SiteQuality
SIO_000300: 1.483e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.07540902940091e-5
allele num: 65032
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.747335313646689e-4
allele num: 11446
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.897070467141726e-5
allele num: 10104
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 1.56e0

ClippingRankSum
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FS
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DP
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
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Other
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South Asian
type: Population
allele count: 0
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Latino
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allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.630744e6

BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.932e1

ReadPosRankSum
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QD
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SIO_000300: 1.646e1

GenotypeDepth
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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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variant carriers: 0