4-10090256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090256
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090256
    reference: chr 4
allele count: 9
allele frequency: 2.741395065488882e-4
allele num: 32830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+32A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+32A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34274
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-10090257-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090257
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090256
    reference: chr 4
allele count: 1
allele frequency: 3.016955288722621e-5
allele num: 33146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+30delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+30delG
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: TC
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

4-10090260-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090260
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090260
    reference: chr 4
allele count: 3
allele frequency: 8.62217623728229e-5
allele num: 34794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+28G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+28G>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34643
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

4-10090261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090261
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090261
    reference: chr 4
allele count: 1
allele frequency: 2.822944896115628e-5
allele num: 35424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+27G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+27G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS

4-10090265-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090265
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090265
    reference: chr 4
allele count: 3
allele frequency: 7.877323810524105e-5
allele num: 38084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+23G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+23G>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34683
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

4-10090265-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090265
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090265
    reference: chr 4
allele count: 1
allele frequency: 2.625774603508035e-5
allele num: 38084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+23G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-10090274-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090274
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090274
    reference: chr 4
allele count: 1
allele frequency: 2.2677793904209e-5
allele num: 44096
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+14T>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+14T>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

4-10090274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090274
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090274
    reference: chr 4
allele count: 30
allele frequency: 6.803338171262699e-4
allele num: 44096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+14T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+14T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 34115
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

4-10090278-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090278
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090278
    reference: chr 4
allele count: 1
allele frequency: 2.152481811528693e-5
allele num: 46458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+10G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+10G>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33407
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

4-10090285-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090285
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090285
    reference: chr 4
allele count: 1
allele frequency: 1.946282600233554e-5
allele num: 51380
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.636+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.371+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.648+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.216+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.308+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.236+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.216+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1575+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.133+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.636+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.292+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.150+3A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.191+3A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.636+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

4-10090291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090291
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090291
    reference: chr 4
allele count: 1
allele frequency: 1.808122084403139e-5
allele num: 55306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.213C>T
  hgvsp: ENST00000502702.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.289C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.645C>T
  hgvsp: ENST00000508079.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.147C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1572C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.188C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.130C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.213C>T
  hgvsp: ENST00000382451.2:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.633C>T
  hgvsp: ENST00000499869.2:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.633C>T
  hgvsp: ENST00000382452.2:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.233C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.368C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.305C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly211Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

4-10090294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090294
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090294
    reference: chr 4
allele count: 4
allele frequency: 6.924248719013987e-5
allele num: 57768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.144C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.630C>T
  hgvsp: ENST00000382452.2:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1569C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.302C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.127C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.365C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.210C>T
  hgvsp: ENST00000502702.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.630C>T
  hgvsp: ENST00000499869.2:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.185C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.642C>T
  hgvsp: ENST00000508079.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.210C>T
  hgvsp: ENST00000382451.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.286C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.230C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp210Asp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

4-10090294-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090294
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090294
    reference: chr 4
allele count: 1
allele frequency: 1.731062179753497e-5
allele num: 57768
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.630C>A
  hgvsp: ENSP00000427687.1:p.Asp210Glu
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.210C>A
  hgvsp: ENSP00000426725.1:p.Asp70Glu
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.630C>A
  hgvsp: ENSP00000371890.2:p.Asp210Glu
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.365C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.144C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.302C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.230C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1569C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.286C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.210C>A
  hgvsp: ENSP00000371889.2:p.Asp70Glu
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.642C>A
  hgvsp: ENSP00000425481.1:p.Asp214Glu
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.185C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.127C>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp210Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

4-10090299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090299
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090299
    reference: chr 4
allele count: 1
allele frequency: 1.647989452867502e-5
allele num: 60680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.180G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.205G>A
  hgvsp: ENSP00000371889.2:p.Ala69Thr
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.139G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.205G>A
  hgvsp: ENSP00000426725.1:p.Ala69Thr
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.360G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.625G>A
  hgvsp: ENSP00000427687.1:p.Ala209Thr
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.225G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.122G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.625G>A
  hgvsp: ENSP00000371890.2:p.Ala209Thr
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.637G>A
  hgvsp: ENSP00000425481.1:p.Ala213Thr
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.297G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.281G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1564G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala209Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

4-10090309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090309
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090309
    reference: chr 4
allele count: 1
allele frequency: 1.580028440511929e-5
allele num: 63290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.195C>T
  hgvsp: ENST00000502702.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.350C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.112C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.615C>T
  hgvsp: ENST00000499869.2:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.627C>T
  hgvsp: ENST00000508079.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.271C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.215C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.287C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.615C>T
  hgvsp: ENST00000382452.2:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.195C>T
  hgvsp: ENST00000382451.2:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.170C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.129C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1554C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala205Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

4-10090317-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090317
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090317
    reference: chr 4
allele count: 1
allele frequency: 1.539314081645219e-5
allele num: 64964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.104A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.162A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.607A>G
  hgvsp: ENSP00000427687.1:p.Arg203Gly
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.187A>G
  hgvsp: ENSP00000371889.2:p.Arg63Gly
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.121A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.279A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.607A>G
  hgvsp: ENSP00000371890.2:p.Arg203Gly
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1546A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.619A>G
  hgvsp: ENSP00000425481.1:p.Arg207Gly
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.187A>G
  hgvsp: ENSP00000426725.1:p.Arg63Gly
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.263A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.207A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.342A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16005
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg203Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

4-10090321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090321
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090321
    reference: chr 4
allele count: 2
allele frequency: 3.075976622577668e-5
allele num: 65020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.603G>A
  hgvsp: ENST00000382452.2:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.259G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.117G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.338G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.615G>A
  hgvsp: ENST00000508079.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.203G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1542G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.100G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.183G>A
  hgvsp: ENST00000502702.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.183G>A
  hgvsp: ENST00000382451.2:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.603G>A
  hgvsp: ENST00000499869.2:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.158G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.275G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26284
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly201Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-10090324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090324
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090324
    reference: chr 4
allele count: 1
allele frequency: 1.537373551025428e-5
allele num: 65046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.256T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1539T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.600T>C
  hgvsp: ENST00000499869.2:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.335T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.155T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.180T>C
  hgvsp: ENST00000502702.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.114T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.97T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.180T>C
  hgvsp: ENST00000382451.2:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.612T>C
  hgvsp: ENST00000508079.1:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.200T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.600T>C
  hgvsp: ENST00000382452.2:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.272T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp200Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

4-10090331-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090331
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090331
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 64390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.265C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.173C>G
  hgvsp: ENSP00000371889.2:p.Ser58Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.593C>G
  hgvsp: ENSP00000371890.2:p.Ser198Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.249C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.90C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.193C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.593C>G
  hgvsp: ENSP00000427687.1:p.Ser198Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1532C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.605C>G
  hgvsp: ENSP00000425481.1:p.Ser202Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.107C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.173C>G
  hgvsp: ENSP00000426725.1:p.Ser58Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.328C>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.148C>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26420
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13954
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser198Cys
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

4-10090333-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090333
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090333
    reference: chr 4
allele count: 1
allele frequency: 1.564064064064064e-5
allele num: 63936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.326C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.191C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.146C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.105C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.603C>T
  hgvsp: ENST00000508079.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.591C>T
  hgvsp: ENST00000382452.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1530C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.591C>T
  hgvsp: ENST00000499869.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.171C>T
  hgvsp: ENST00000382451.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.263C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.247C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.88C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.171C>T
  hgvsp: ENST00000502702.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe197Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-10090342-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090342
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090341
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 61374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.161delG
  hgvsp: ENSP00000371889.2:p.Cys54LeufsTer72
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.581delG
  hgvsp: ENSP00000427687.1:p.Cys194LeufsTer72
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.161delG
  hgvsp: ENSP00000426725.1:p.Cys54LeufsTer72
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1520delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.237delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.78delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.253delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.581delG
  hgvsp: ENSP00000371890.2:p.Cys194LeufsTer72
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.316delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.95delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.593delG
  hgvsp: ENSP00000425481.1:p.Cys198LeufsTer47
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.181delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.136delG
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27096
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys194LeufsTer72
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AC
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

4-10090355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090355
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090355
    reference: chr 4
allele count: 1
allele frequency: 1.780880467303035e-5
allele num: 56152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.241G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.66G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.581G>A
  hgvsp: ENSP00000425481.1:p.Arg194His
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.569G>A
  hgvsp: ENSP00000427687.1:p.Arg190His
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.225G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1508G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.169G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.569G>A
  hgvsp: ENSP00000371890.2:p.Arg190His
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.149G>A
  hgvsp: ENSP00000426725.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.149G>A
  hgvsp: ENSP00000371889.2:p.Arg50His
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.124G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.304G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.83G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27213
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg190His
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

4-10090359-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090359
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090359
    reference: chr 4
allele count: 3
allele frequency: 5.462291977713849e-5
allele num: 54922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.300A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.565A>T
  hgvsp: ENSP00000427687.1:p.Ser189Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.165A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.145A>T
  hgvsp: ENSP00000426725.1:p.Ser49Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.565A>T
  hgvsp: ENSP00000371890.2:p.Ser189Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.145A>T
  hgvsp: ENSP00000371889.2:p.Ser49Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.577A>T
  hgvsp: ENSP00000425481.1:p.Ser193Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1504A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.221A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.62A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.79A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.237A>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.120A>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27137
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser189Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-10090361-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090361
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090361
    reference: chr 4
allele count: 1
allele frequency: 1.85508106704263e-5
allele num: 53906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.143A>G
  hgvsp: ENSP00000371889.2:p.His48Arg
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1502A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.575A>G
  hgvsp: ENSP00000425481.1:p.His192Arg
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.163A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.118A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.563A>G
  hgvsp: ENSP00000427687.1:p.His188Arg
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.563A>G
  hgvsp: ENSP00000371890.2:p.His188Arg
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.219A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.143A>G
  hgvsp: ENSP00000426725.1:p.His48Arg
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.77A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.60A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.298A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.235A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12666
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His188Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

4-10090363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090363
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090363
    reference: chr 4
allele count: 1
allele frequency: 1.89000189000189e-5
allele num: 52910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.573C>T
  hgvsp: ENST00000508079.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.161C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.561C>T
  hgvsp: ENST00000382452.2:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.296C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.141C>T
  hgvsp: ENST00000382451.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.58C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.75C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.233C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.217C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.116C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1500C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.141C>T
  hgvsp: ENST00000502702.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.561C>T
  hgvsp: ENST00000499869.2:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12646
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.561C>T
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

4-10090372-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090372
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090372
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 49110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-7C>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-7C>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25619
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.559-7C>A
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

4-10090373-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090373
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090373
    reference: chr 4
allele count: 1
allele frequency: 2.046831504830522e-5
allele num: 48856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-8T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12156
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.559-8T>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

4-10090377-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090377
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090377
    reference: chr 4
allele count: 1
allele frequency: 2.175142471831905e-5
allele num: 45974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-12G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-12G>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

4-10090382-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090382
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090382
    reference: chr 4
allele count: 1
allele frequency: 2.325473233803079e-5
allele num: 43002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-17T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14986
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-10090382-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090382
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090381
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 43002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-18delG
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-18delG
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14986
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22737
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: AC
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

4-10090383-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090383
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090383
    reference: chr 4
allele count: 1
allele frequency: 2.344995779007598e-5
allele num: 42644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-18G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-18G>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

4-10090384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090384
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090384
    reference: chr 4
allele count: 1
allele frequency: 2.3857238286096e-5
allele num: 41916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-19G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-19G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-10090385-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090385
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090385
    reference: chr 4
allele count: 1
allele frequency: 2.414759007051096e-5
allele num: 41412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-20A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-20A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

4-10090388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090388
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090388
    reference: chr 4
allele count: 3
allele frequency: 7.70257779603574e-5
allele num: 38948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-23G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-23G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21550
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

4-10090400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090400
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090400
    reference: chr 4
allele count: 2
allele frequency: 6.723593088146305e-5
allele num: 29746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-35G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20834
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22620
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

4-10090401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090401
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090401
    reference: chr 4
allele count: 1
allele frequency: 3.422547744541036e-5
allele num: 29218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-36C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-36C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20909
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

4-10090405-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090405
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090405
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 27708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-40C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-40C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21085
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22932
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-10090409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090409
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090409
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 27224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-44C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21197
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-10090414-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10090414
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10090414
    reference: chr 4
allele count: 1
allele frequency: 3.764209892343597e-5
allele num: 26566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.114-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.159-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000506246
  gene symbol: WDR1
  hgvsc: ENST00000506246.1:n.73-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.294-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.215-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.231-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.1498-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.56-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-49A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-49A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21255
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-10094622-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094622
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094622
    reference: chr 4
allele count: 1
allele frequency: 9.184423218221895e-5
allele num: 10888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3328G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1685G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000515743
  gene symbol: WDR1
  hgvsc: ENST00000515743.1:n.22G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4257G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4257G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4257G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4257G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.113+45G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4257G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000504739
  gene symbol: WDR1
  hgvsc: ENST00000504739.1:n.37G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3423G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2947G>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

4-10094662-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094662
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094662
    reference: chr 4
allele count: 1
allele frequency: 9.154155986818015e-5
allele num: 10924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1645G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3288G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.113+5G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4297G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4297G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3383G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4297G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4297G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2907G>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4297G>C
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
hgvs: n.113+5G>C
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-10094671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094671
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094671
    reference: chr 4
allele count: 3306
allele frequency: 2.983216025988089e-1
allele num: 11082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4306C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4306C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4306C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.109C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4306C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3279C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1636C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4306C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3374C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2898C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.5e0
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.5e0
  variant carriers: 405
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 9.75e1
  variant carriers: 1779
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 177
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 6.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 9.75e1
  variant carriers: 2713
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 47
num of homozygotes: 531
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

4-10094673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094673
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094673
    reference: chr 4
allele count: 2
allele frequency: 1.822157434402332e-4
allele num: 10976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4308C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4308C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4308C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4308C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3372C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.107C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1634C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4308C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3277C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2896C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

4-10094680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094680
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094680
    reference: chr 4
allele count: 2
allele frequency: 1.824151769427216e-4
allele num: 10964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.100C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3270C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4315C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4315C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1627C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4315C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2889C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4315C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3365C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4315C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4199
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

4-10094697-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094697
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094697
    reference: chr 4
allele count: 1
allele frequency: 9.132420091324201e-5
allele num: 10950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3253C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.83C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2872C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4332C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4332C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4332C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1610C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4332C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4332C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3348C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

4-10094698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094698
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094698
    reference: chr 4
allele count: 2085
allele frequency: 1.897524572260648e-1
allele num: 10988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4333C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4333C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2871C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3347C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.82C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1609C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4333C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3252C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4333C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4333C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 2.5e0
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 9.75e1
  variant carriers: 1318
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 6.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 7.5e0
  variant carriers: 84
num of homozygotes: 214
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

4-10094700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094700
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094700
    reference: chr 4
allele count: 1
allele frequency: 9.139097057210747e-5
allele num: 10942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4335G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3250G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.80G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1607G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4335G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4335G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4335G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2869G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4335G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3345G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-10094704-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094704
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094705
    reference: chr 4
allele count: 1
allele frequency: 9.145783793671118e-5
allele num: 10934
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4340dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4340dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3340dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4340dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.75dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4340dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3245dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2864dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4340dupA
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1602dupA
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-10094736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094736
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094736
    reference: chr 4
allele count: 1
allele frequency: 9.154155986818015e-5
allele num: 10924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3214C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4371C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4371C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1571C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4371C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4371C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2833C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.44C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4371C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3309C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-10094737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094737
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094737
    reference: chr 4
allele count: 1
allele frequency: 9.154155986818015e-5
allele num: 10924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3213G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4372G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1570G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.43G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2832G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4372G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3308G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4372G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4372G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4372G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3557
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

4-10094738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094738
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094738
    reference: chr 4
allele count: 2
allele frequency: 1.830831197363603e-4
allele num: 10924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3307C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4373C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3212C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1569C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4373C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4373C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4373C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4373C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.42C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2831C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3671
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

4-10094745-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094745
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094745
    reference: chr 4
allele count: 2
allele frequency: 1.831501831501832e-4
allele num: 10920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2824G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4380G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3300G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4380G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4380G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1562G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.35G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4380G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3205G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4380G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

4-10094746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094746
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094746
    reference: chr 4
allele count: 49
allele frequency: 4.487179487179487e-3
allele num: 10920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3204C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4381C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4381C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4381C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.34C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4381C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4381C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1561C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3299C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2823C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

4-10094762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10094762
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10094762
    reference: chr 4
allele count: 1
allele frequency: 9.154155986818015e-5
allele num: 10924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000502962
  gene symbol: WDR1
  hgvsc: ENST00000502962.1:n.18C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505543
  gene symbol: WDR1
  hgvsc: ENST00000505543.1:n.293+3188C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.559-4397C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000508949
  gene symbol: WDR1
  hgvsc: ENST00000508949.1:n.158+3283C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-4397C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.559-4397C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.571-4397C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-4397C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000509695
  gene symbol: WDR1
  hgvsc: ENST00000509695.1:n.214+1545C>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000510848
  gene symbol: WDR1
  hgvsc: ENST00000510848.1:n.230+2807C>T
  variant of: http://identifiers.org/hgnc/12754
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/4-10099291-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099291
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099291
    reference: chr 4
allele count: 1
allele frequency: 8.901073469460416e-6
allele num: 112346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+44G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+44G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+44G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8926G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8926G>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6301
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

4-10099293-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099293
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099293
    reference: chr 4
allele count: 11
allele frequency: 9.776213583604401e-5
allele num: 112518
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8928A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+42A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8928A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+42A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+42A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15677
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15508
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3687
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1843
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2999
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6429
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

4-10099297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099297
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099297
    reference: chr 4
allele count: 1
allele frequency: 8.883992821733801e-6
allele num: 112562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+38G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+38G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8932G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8932G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+38G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16524
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2613
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6494
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-10099304-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099304
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099304
    reference: chr 4
allele count: 7
allele frequency: 6.186696834178849e-5
allele num: 113146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8939G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8939G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+31G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+31G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+31G>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18345
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4713
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9485
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1471
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
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genotype quality: GenotypeQuality
  all individuals: 6720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-10099304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099304
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099304
    reference: chr 4
allele count: 1
allele frequency: 8.838138334541212e-6
allele num: 113146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+31G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+31G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+31G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8939G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8939G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 299
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1979
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 378
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

4-10099306-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099306
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099306
    reference: chr 4
allele count: 1
allele frequency: 8.819742110740682e-6
allele num: 113382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+29T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8941T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8941T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+29T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+29T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4755
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18802
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

4-10099313-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099313
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099313
    reference: chr 4
allele count: 3
allele frequency: 2.631209654785293e-5
allele num: 114016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+22G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+22G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+22G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8948G>A
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8948G>A
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3071
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4855
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/4-10099315-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099315
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099314
    reference: chr 4
allele count: 2
allele frequency: 1.747549062439928e-5
allele num: 114446
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+19delT
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8951delT
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+19delT
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8951delT
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+19delT
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19577
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4905
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2812
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9584
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2046
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7001
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: CA
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

4-10099317-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099317
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099317
    reference: chr 4
allele count: 1
allele frequency: 8.702008423544154e-6
allele num: 114916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8952T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+18T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+18T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+18T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8952T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19981
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

4-10099318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099318
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099318
    reference: chr 4
allele count: 12
allele frequency: 1.042245692051139e-4
allele num: 115136
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8953T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8953T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+17T>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+17T>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14725
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20173
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4939
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21048
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

4-10099331-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099331
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099331
    reference: chr 4
allele count: 1
allele frequency: 8.509769215058888e-6
allele num: 117512
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.558+4A>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.558+4A>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8966A>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.570+4A>C
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8966A>C
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5061
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 2.25e1
  variant carriers: 0
hgvs: c.558+4A>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/4-10099336-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099336
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099336
    reference: chr 4
allele count: 1
allele frequency: 8.430281571404485e-6
allele num: 118620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8971G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.557G>T
  hgvsp: ENSP00000427687.1:p.Gly186Val
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.557G>T
  hgvsp: ENSP00000371890.2:p.Gly186Val
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505851
  gene symbol: WDR1
  hgvsc: ENST00000505851.1:n.715G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000264785
  gene symbol: WDR1
  hgvsc: ENST00000264785.7:n.547G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.569G>T
  hgvsp: ENSP00000425481.1:p.Gly190Val
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8971G>T
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7468
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5115
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly186Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/4-10099337-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099337
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099337
    reference: chr 4
allele count: 1
allele frequency: 8.415383320710258e-6
allele num: 118830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8972G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505851
  gene symbol: WDR1
  hgvsc: ENST00000505851.1:n.714G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.556G>T
  hgvsp: ENSP00000371890.2:p.Gly186Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.568G>T
  hgvsp: ENSP00000425481.1:p.Gly190Cys
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000264785
  gene symbol: WDR1
  hgvsc: ENST00000264785.7:n.546G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8972G>T
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.556G>T
  hgvsp: ENSP00000427687.1:p.Gly186Cys
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9686
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4335
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly186Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

4-10099340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10099340
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 10099340
    reference: chr 4
allele count: 78121
allele frequency: 6.491905996543013e-1
allele num: 120336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371889
  ensembl transcript: ENST00000382451
  gene symbol: WDR1
  hgvsc: ENST00000382451.2:c.139-8975A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000371890
  ensembl transcript: ENST00000382452
  gene symbol: WDR1
  hgvsc: ENST00000382452.2:c.553A>G
  hgvsp: ENSP00000371890.2:p.Ile185Val
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000264785
  gene symbol: WDR1
  hgvsc: ENST00000264785.7:n.543A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000425481
  ensembl transcript: ENST00000508079
  gene symbol: WDR1
  hgvsc: ENST00000508079.1:c.565A>G
  hgvsp: ENSP00000425481.1:p.Ile189Val
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000427687
  ensembl transcript: ENST00000499869
  gene symbol: WDR1
  hgvsc: ENST00000499869.2:c.553A>G
  hgvsp: ENSP00000427687.1:p.Ile185Val
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071127
  ensembl protein: ENSP00000426725
  ensembl transcript: ENST00000502702
  gene symbol: WDR1
  hgvsc: ENST00000502702.1:c.139-8975A>G
  variant of: http://identifiers.org/hgnc/12754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071127
  ensembl transcript: ENST00000505851
  gene symbol: WDR1
  hgvsc: ENST00000505851.1:n.711A>G
  variant of: http://identifiers.org/hgnc/12754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 6.75e1
  variant carriers: 4669
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 9.25e1
  variant carriers: 2095
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 8.75e1
  variant carriers: 2769
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 4.75e1
  variant carriers: 2636
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 8.25e1
  variant carriers: 3233
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.75e1
  variant carriers: 4047
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 2.25e1
  variant carriers: 1318
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 5.25e1
  variant carriers: 3430
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.25e1
  variant carriers: 1747
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 6.25e1
  variant carriers: 4576
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 2.75e1
  variant carriers: 1646
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 3.75e1
  variant carriers: 1816
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.75e1
  variant carriers: 688
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 4.25e1
  variant carriers: 2160
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 7.75e1
  variant carriers: 3809
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 9.75e1
  variant carriers: 7019
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 7.25e1
  variant carriers: 4420
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.25e1
  variant carriers: 164
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 8.25e1
  variant carriers: 330
genotype quality: GenotypeQuality
  all individuals: 6459
  bin: 6.25e1
  variant carriers: 221
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 111
hgvs: p.Ile185Val
num of homozygotes: 25821
reference allele: T

GenotypeDepth
all individuals: 334
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 732
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32060
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4987
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 9.75e1
variant carriers: 11

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1798
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 1.071173530111878e-3
allele num: 8402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16056
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.313e1

FS
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

DP
type: SiteQuality
SIO_000300: 7.14718e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

GenotypeDepth
all individuals: 18
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2384
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1068
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32243
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8734
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.162188809465122e-5
allele num: 16228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3172
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.077e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

QD
type: SiteQuality
SIO_000300: 1.18e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

FS
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 7.18771e5

GenotypeDepth
all individuals: 47
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1401
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1390
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7739
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1842
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32801
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.21654501216545e-3
allele num: 1644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.799791207516529e-5
allele num: 17242
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

FS
type: SiteQuality
SIO_000300: 1.837e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

DP
type: SiteQuality
SIO_000300: 7.34164e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

QD
type: SiteQuality
SIO_000300: 3.318e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.141e0

GenotypeDepth
all individuals: 707
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1532
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2011
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7414
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5595
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1682
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.668291576918717e-5
allele num: 17642
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1918
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.178e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.893e0

VQSLOD
type: SiteQuality
SIO_000300: -1.542e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

DP
type: SiteQuality
SIO_000300: 7.39357e5

FS
type: SiteQuality
SIO_000300: 1.2241e1

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2153
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 388
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33660
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1401
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.557147306135161e-4
allele num: 19266
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2074
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2262
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.333e1

DP
type: SiteQuality
SIO_000300: 7.62649e5

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33660
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.190491020450534e-5
allele num: 19266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2074
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1970
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.333e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 7.62649e5

GenotypeDepth
all individuals: 1067
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 21
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8965
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33879
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2366
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22940
num of homozygotes: 0

Latino
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allele num: 2546
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -5.1e-1

FS
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SIO_000300: 5.42e-1

MQRankSum
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InbreedingCoeff
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VQSLOD
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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: 4.06e-1

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 10

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

European (Non-Finnish)
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allele count: 2
allele frequency: 8.718395815170009e-5
allele num: 22940
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2546
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 5.263157894736842e-3
allele num: 380
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2366
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.48015873015873e-4
allele num: 4032
num of homozygotes: 0

South Asian
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allele count: 25
allele frequency: 2.782105497440463e-3
allele num: 8986
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East Asian
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allele count: 0
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ClippingRankSum
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SIO_000300: 4.06e-1

MQRankSum
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FS
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DP
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: -5.1e-1

InbreedingCoeff
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SIO_000300: 9.8e-3

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

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

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

Latino
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allele count: 1
allele frequency: 3.571428571428571e-4
allele num: 2800
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 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: 4224
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

ReadPosRankSum
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SIO_000300: 0.0e0

InbreedingCoeff
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QD
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SIO_000300: 1.029e1

ClippingRankSum
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FS
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SIO_000300: 1.391e0

VQSLOD
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MQ
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SIO_000300: 5.747e1

DP
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SIO_000300: 8.3443e5

MQRankSum
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SIO_000300: 2.5e-1

BaseQRankSum
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SIO_000300: -1.799e0

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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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
all individuals: 11825
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.6405999708752e-5
allele num: 27468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
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
type: Population
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3574
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

FS
type: SiteQuality
SIO_000300: 2.963e0

MQRankSum
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SIO_000300: 4.29e-1

QD
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VQSLOD
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BaseQRankSum
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SIO_000300: 3.0e0

ClippingRankSum
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SIO_000300: -1.286e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -7.5e-3

DP
type: SiteQuality
SIO_000300: 8.75194e5

ReadPosRankSum
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SIO_000300: 1.41e0

GenotypeDepth
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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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele 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: 3.335334534053766e-5
allele num: 29982
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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QD
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GenotypeDepth
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variant carriers: 1

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: 2.75e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4094
num of homozygotes: 0

African
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allele frequency: 1.998401278976818e-4
allele num: 5004
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 2.43427458617332e-4
allele num: 4108
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31448
num of homozygotes: 0

South Asian
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allele frequency: 2.077274615704196e-4
allele num: 9628
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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QD
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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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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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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3014
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 31448
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 9.32727e5

QD
type: SiteQuality
SIO_000300: 8.48e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1695
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.010959894014212e-5
allele num: 33212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

FS
type: SiteQuality
SIO_000300: 4.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

BaseQRankSum
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SIO_000300: -4.0e-1

DP
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SIO_000300: 9.52352e5

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16661
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variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3242
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.86219739292365e-4
allele num: 5370
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 9.70474e5

FS
type: SiteQuality
SIO_000300: 3.783e0

QD
type: SiteQuality
SIO_000300: 1.399e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.797985450475658e-5
allele num: 35740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3304
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 9.8086e5

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: -1.408e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
all individuals: 858
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.593779716954746e-5
allele num: 35754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5518
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3292
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.002e1

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 9.79816e5

InbreedingCoeff
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SIO_000300: -5.4e-3

MQRankSum
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SIO_000300: -3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

GenotypeDepth
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variant carriers: 1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.79376431804213e-5
allele num: 35794
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 count: 0
allele frequency: 0.0e0
allele num: 5512
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 count: 0
allele frequency: 0.0e0
allele num: 5068
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

BaseQRankSum
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SIO_000300: 8.31e-1

FS
type: SiteQuality
SIO_000300: 2.398e0

ClippingRankSum
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SIO_000300: -3.8e-1

ReadPosRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.75797e5

GenotypeDepth
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variant carriers: 0

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: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4604
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35394
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.897e0

VQSLOD
type: SiteQuality
SIO_000300: 4.09e-1

InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.62121e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeDepth
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variant carriers: 0

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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allele count: 0
allele frequency: 0.0e0
allele num: 5382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4906
num of homozygotes: 0

East Asian
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allele frequency: 2.201673271686482e-4
allele num: 4542
num of homozygotes: 0

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

FS
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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SIO_000300: -5.89e-1

VQSLOD
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BaseQRankSum
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GenotypeDepth
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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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East 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 frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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BaseQRankSum
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SIO_000300: -9.370000000000001e-1

ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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GenotypeDepth
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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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Latino
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allele frequency: 0.0e0
allele num: 4070
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 474
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 3.295544423938835e-5
allele num: 30344
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.059e0

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

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 count: 0
allele frequency: 0.0e0
allele num: 29616
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 count: 0
allele frequency: 0.0e0
allele num: 4760
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 2.556237218813906e-4
allele num: 3912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
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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

East Asian
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allele count: 2
allele frequency: 5.473453749315818e-4
allele num: 3654
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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FS
type: SiteQuality
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DP
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.64e0

ReadPosRankSum
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SIO_000300: 4.21e-1

GenotypeDepth
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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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allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 9562
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Latino
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num of homozygotes: 0

Other
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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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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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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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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Other
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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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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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
all individuals: 60
bin: 4.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 25976
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3010
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3262
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.315886984715146e-4
allele num: 4318
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
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SIO_000300: -2.08e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.149e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 7.51192e5

MQRankSum
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SIO_000300: -3.77e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.01e-1

QD
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SIO_000300: 7.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

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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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24230
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2926
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 3.631082062454611e-4
allele num: 2754
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

DP
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SIO_000300: 7.25447e5

MQ
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ReadPosRankSum
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SIO_000300: -7.66e-1

FS
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SIO_000300: 2.363e0

ClippingRankSum
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SIO_000300: 1.77e-1

BaseQRankSum
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SIO_000300: -4.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.925e-1

QD
type: SiteQuality
SIO_000300: 7.61e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.116071428571429e-4
allele num: 8960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22394
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
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SIO_000300: 4.78e0

FS
type: SiteQuality
SIO_000300: 4.749e0

QD
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SIO_000300: 1.479e1

ClippingRankSum
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SIO_000300: -9.56e-1

InbreedingCoeff
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SIO_000300: 2.48e-2

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 7.04681e5

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

InbreedingCoeff
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SIO_000300: 2.48e-2

FS
type: SiteQuality
SIO_000300: 4.749e0

VQSLOD
type: SiteQuality
SIO_000300: 8.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.04681e5

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

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
all individuals: 2142
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3868
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2432
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2550
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2330
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8940
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.516711833785005e-5
allele num: 22140
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

InbreedingCoeff
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VQSLOD
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MQ
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DP
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ClippingRankSum
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SIO_000300: 7.06e-1

ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
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SIO_000300: 4.521e0

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

African
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allele 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: 4.608294930875576e-5
allele num: 21700
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

FS
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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ClippingRankSum
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SIO_000300: 1.93e-1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 4.683402023229674e-5
allele num: 21352
num of homozygotes: 0

European (Finnish)
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East Asian
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Other
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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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FS
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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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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: 2

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3564
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

East Asian
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allele count: 3
allele frequency: 1.449275362318841e-3
allele num: 2070
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2208
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 19900
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

VQSLOD
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SIO_000300: 7.1e-1

BaseQRankSum
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SIO_000300: -9.56e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

DP
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SIO_000300: 6.70168e5

FS
type: SiteQuality
SIO_000300: 8.952e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.56e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2890
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 14094
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 1.628664495114007e-3
allele num: 1228
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.813e-1

ReadPosRankSum
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FS
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SIO_000300: 7.748e0

ClippingRankSum
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SIO_000300: -4.21e-1

InbreedingCoeff
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SIO_000300: -4.5e-2

MQRankSum
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SIO_000300: 4.21e-1

DP
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SIO_000300: 6.03283e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.02e0

QD
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SIO_000300: 1.4e1

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 7.266385699752942e-5
allele num: 13762
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.00109e5

ClippingRankSum
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SIO_000300: -3.11e-1

InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 7.2e-1

MQRankSum
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FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.316e1

VQSLOD
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SIO_000300: 4.81e0

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12882
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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

Latino
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InbreedingCoeff
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SIO_000300: -5.04e-2

FS
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SIO_000300: 0.0e0

DP
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QD
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MQRankSum
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SIO_000300: 5.29e-1

BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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SIO_000300: -5.298e-1

ReadPosRankSum
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SIO_000300: 7.31e-1

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: 0

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

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

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

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

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

Latino
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -4.82e-2

ClippingRankSum
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SIO_000300: 7.2e-1

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: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 950
num of homozygotes: 0

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

Latino
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allele frequency: 1.196172248803828e-3
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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

Other
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African
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South Asian
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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FS
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DP
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QD
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ReadPosRankSum
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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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GenotypeQuality
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African
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allele frequency: 4.716981132075472e-3
allele num: 212
num of homozygotes: 0

Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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DP
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ReadPosRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2359
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.518648838845883e-4
allele num: 2842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.406e0

QD
type: SiteQuality
SIO_000300: 1.272e1

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.43509e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 21

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 17

GenotypeQuality
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bin: 6.25e1
variant carriers: 31

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 143

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 21

GenotypeQuality
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GenotypeQuality
all individuals: 236
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variant carriers: 22

East Asian
type: Population
allele count: 39
allele frequency: 2.4375e-1
allele num: 160
num of homozygotes: 8

Other
type: Population
allele count: 39
allele frequency: 3.25e-1
allele num: 120
num of homozygotes: 6

European (Finnish)
type: Population
allele count: 11
allele frequency: 5.0e-1
allele num: 22
num of homozygotes: 2

African
type: Population
allele count: 54
allele frequency: 2.454545454545455e-1
allele num: 220
num of homozygotes: 7

Latino
type: Population
allele count: 25
allele frequency: 2.659574468085106e-1
allele num: 94
num of homozygotes: 2

South Asian
type: Population
allele count: 1927
allele frequency: 2.567279509725553e-1
allele num: 7506
num of homozygotes: 253

European (Non-Finnish)
type: Population
allele count: 1211
allele frequency: 4.091216216216216e-1
allele num: 2960
num of homozygotes: 253

QD
type: SiteQuality
SIO_000300: 1.728e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.513e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

DP
type: SiteQuality
SIO_000300: 4.19985e5

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
all individuals: 442
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2884
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.578947368421052e-3
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 8.474576271186441e-3
allele num: 118
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.48e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 1.085e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.758e0

VQSLOD
type: SiteQuality
SIO_000300: -4.681e-1

DP
type: SiteQuality
SIO_000300: 2.95417e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

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
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.77e-2

QD
type: SiteQuality
SIO_000300: 1.725e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 2.94408e5

MQ
type: SiteQuality
SIO_000300: 5.912e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.28e0

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

FS
type: SiteQuality
SIO_000300: 1.117e0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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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: 24
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GenotypeQuality
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GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 3180
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GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2866
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.41e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: -1.08e0

FS
type: SiteQuality
SIO_000300: 2.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.33e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

DP
type: SiteQuality
SIO_000300: 2.93652e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-1

QD
type: SiteQuality
SIO_000300: 8.75e0

GenotypeQuality
all individuals: 202
bin: 8.25e1
variant carriers: 11

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 30

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 51

GenotypeQuality
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GenotypeQuality
all individuals: 756
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GenotypeQuality
all individuals: 242
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variant carriers: 13

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 171
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GenotypeQuality
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GenotypeQuality
all individuals: 99
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1863

GenotypeQuality
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GenotypeQuality
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variant carriers: 27

GenotypeQuality
all individuals: 171
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GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 13

South Asian
type: Population
allele count: 1134
allele frequency: 1.510791366906475e-1
allele num: 7506
num of homozygotes: 97

European (Finnish)
type: Population
allele count: 5
allele frequency: 3.571428571428572e-1
allele num: 14
num of homozygotes: 0

Other
type: Population
allele count: 30
allele frequency: 2.5e-1
allele num: 120
num of homozygotes: 4

Latino
type: Population
allele count: 19
allele frequency: 2.021276595744681e-1
allele num: 94
num of homozygotes: 1

East Asian
type: Population
allele count: 24
allele frequency: 1.558441558441558e-1
allele num: 154
num of homozygotes: 3

African
type: Population
allele count: 15
allele frequency: 7.211538461538461e-2
allele num: 208
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 858
allele frequency: 2.966804979253112e-1
allele num: 2892
num of homozygotes: 108

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.46e-2

QD
type: SiteQuality
SIO_000300: 1.309e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.19e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.463e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

DP
type: SiteQuality
SIO_000300: 3.9485e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-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
all individuals: 250
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.785e1

FS
type: SiteQuality
SIO_000300: 7.495e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.941e0

DP
type: SiteQuality
SIO_000300: 2.65598e5

VQSLOD
type: SiteQuality
SIO_000300: -1.372e0

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

QD
type: SiteQuality
SIO_000300: 7.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.761904761904762e-3
allele num: 210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.52e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.65214e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.694e0

FS
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SIO_000300: 7.804e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

MQRankSum
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SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.03e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2995
bin: 9.75e1
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GenotypeQuality
all individuals: 340
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 120
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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

QD
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DP
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FS
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.87e-2

MQRankSum
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SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.076e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2844
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 150
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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

Other
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allele frequency: 8.333333333333333e-3
allele num: 120
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.869e1

QD
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
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SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 2.6367e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 94
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2842
num of homozygotes: 0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.205e0

BaseQRankSum
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SIO_000300: -9.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
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SIO_000300: -2.004e0

QD
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SIO_000300: 1.232e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
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allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2842
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 150
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.126e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
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SIO_000300: -4.76e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 1.172e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 2.63516e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 49

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2842
num of homozygotes: 0

South Asian
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allele count: 48
allele frequency: 6.394884092725819e-3
allele num: 7506
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.063829787234043e-2
allele num: 94
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 2
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East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-2

ClippingRankSum
type: SiteQuality
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 6.666666666666667e-3
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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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VQSLOD
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FS
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 64182
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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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FS
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QD
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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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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European (Non-Finnish)
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South Asian
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allele frequency: 7.81114389862871e-4
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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FS
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Other
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African
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European (Non-Finnish)
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Latino
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.761170492377782e-5
allele num: 11414
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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South Asian
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.644614e6

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

GenotypeQuality
all individuals: 3977
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551349674216568e-5
allele num: 64460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 9.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

DP
type: SiteQuality
SIO_000300: 1.644614e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.395e0

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4027
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GenotypeQuality
all individuals: 1359
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11962
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.74737578726382e-5
allele num: 11432
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: -2.125e0

MQRankSum
type: SiteQuality
SIO_000300: -1.893e0

QD
type: SiteQuality
SIO_000300: 1.399e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 3.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.534e0

DP
type: SiteQuality
SIO_000300: 1.650104e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.498950314905528e-4
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64698
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.210000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.565e0

DP
type: SiteQuality
SIO_000300: 1.671937e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

FS
type: SiteQuality
SIO_000300: 3.848e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542828931128116e-5
allele num: 64816
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

QD
type: SiteQuality
SIO_000300: 1.27e1

FS
type: SiteQuality
SIO_000300: 6.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e0

DP
type: SiteQuality
SIO_000300: 1.680168e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53950366401872e-5
allele num: 64956
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12874
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 2.546e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

DP
type: SiteQuality
SIO_000300: 1.685861e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.614e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 693
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3459
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9616
bin: 9.75e1
variant carriers: 12

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.076691174208632e-4
allele num: 65014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13004
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.359197907585005e-4
allele num: 11470
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.688581e6

QD
type: SiteQuality
SIO_000300: 1.36e1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.907e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9649
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2868
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variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522579859313621e-5
allele num: 65678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14516
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.72035e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e0

FS
type: SiteQuality
SIO_000300: 7.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 75
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.559097468188377e-5
allele num: 15246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66000
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

QD
type: SiteQuality
SIO_000300: 2.861e1

DP
type: SiteQuality
SIO_000300: 1.733576e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.494e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15382
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.702e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.272e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.422e0

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 1.736356e6

QD
type: SiteQuality
SIO_000300: 1.112e1

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
all individuals: 1212
bin: 6.75e1
variant carriers: 262

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 157

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 25
bin: 7.5e0
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GenotypeQuality
all individuals: 147
bin: 2.25e1
variant carriers: 20

GenotypeQuality
all individuals: 49956
bin: 9.75e1
variant carriers: 49916

GenotypeQuality
all individuals: 474
bin: 7.75e1
variant carriers: 315

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 48