15-85189166-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189166
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189166
    reference: chr 15
allele count: 1
allele frequency: 2.258661968649772e-5
allele num: 44274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-99C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-99C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-99C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-99C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.741+38C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1111C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4091C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.766C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-99C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*93+38C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-99C>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13857
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

15-85189178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189178
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189178
    reference: chr 15
allele count: 1
allele frequency: 3.051571559353067e-5
allele num: 32770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*93+26G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-111G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.754G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.741+26G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4079G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-111G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-111G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1099G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-111G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-111G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-111G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

15-85189196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189196
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189196
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 20726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4061G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-129G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*93+8G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-129G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-129G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1081G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-129G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.741+8G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-129G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.736G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-129G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*93+8G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

15-85189199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189199
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189199
    reference: chr 15
allele count: 1
allele frequency: 4.944620253164557e-5
allele num: 20224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-132G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4058G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.733G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1078G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-132G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-132G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*93+5G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-132G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.741+5G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-132G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-132G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*93+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

15-85189204-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189204
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189204
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 19026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.741G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*93G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-137G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4053G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-137G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-137G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1073G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-137G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.728G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-137G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-137G>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*93G>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD

15-85189206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189206
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189206
    reference: chr 15
allele count: 5
allele frequency: 2.670654844567888e-4
allele num: 18722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.726A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1071A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-139A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*91A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-139A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-139A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.739A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-139A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-139A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4051A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-139A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15214
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*91A>G
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

15-85189210-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189210
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189210
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 17760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-143G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1067G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.735G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-143G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.722G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-143G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-143G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*87G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4047G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-143G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-143G>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14166
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

15-85189226-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189226
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189226
    reference: chr 15
allele count: 1
allele frequency: 6.097560975609756e-5
allele num: 16400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-159C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*531C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-159C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4031C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.706C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-159C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-159C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*71C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-159C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1051C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-159C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.719C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12034
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33674
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

15-85189235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189235
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189235
    reference: chr 15
allele count: 1
allele frequency: 6.347594261774788e-5
allele num: 15754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.697G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.594-168G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1106-168G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.710G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*165-168G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1042G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*522G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*62G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.982-168G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4022G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1024-168G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.518-168G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/15-85189241-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189241
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189241
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 15702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*56T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+174T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*516T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+174T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.704T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+174T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+174T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.691T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1036T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+174T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+174T>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.4016T>G
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11099
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33839
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

15-85189263-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189263
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189263
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 15410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+152A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3994A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*494A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+152A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+152A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*34A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+152A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.682A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1014A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+152A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+152A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.669A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

15-85189264-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189264
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189264
    reference: chr 15
allele count: 1
allele frequency: 6.469979296066253e-5
allele num: 15456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*33T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*493T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+151T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1013T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+151T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3993T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+151T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.681T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+151T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+151T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.668T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+151T>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

15-85189268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189268
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189268
    reference: chr 15
allele count: 1
allele frequency: 6.47332988089073e-5
allele num: 15448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.664C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+147C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.582C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+147C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+147C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.677C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3989C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+147C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+147C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+147C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1009C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

15-85189277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189277
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189277
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 15798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+138C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+138C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*480C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.1000C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+138C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+138C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+138C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3980C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.655C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.573C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+138C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.668C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15739
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

15-85189279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189279
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189279
    reference: chr 15
allele count: 1
allele frequency: 6.345982992765579e-5
allele num: 15758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.666G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+136G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+136G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.571G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3978G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+136G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*478G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+136G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+136G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.998G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.653G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+136G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-85189284-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189284
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189284
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 16252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+131C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.648C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*473C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.993C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.661C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+131C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+131C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3973C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.566C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+131C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+131C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+131C>G
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30073
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18409
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

15-85189293-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189293
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189293
    reference: chr 15
allele count: 2
allele frequency: 1.157943492357573e-4
allele num: 17272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.984A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+122A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.639A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.*4A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*464A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+122A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+122A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.557A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3964A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.652A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+122A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+122A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+122A>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22671
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

15-85189302-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189302
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189302
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 18652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.975C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+113C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+113C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+113C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+113C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.630C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.548C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3955C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.531C>T
  hgvsp: ENSP00000453732.1:p.Gln178Ter
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*455C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+113C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.643C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+113C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: stop gained
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27488
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln178Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

15-85189304-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189304
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189304
    reference: chr 15
allele count: 2
allele frequency: 1.042970379641218e-4
allele num: 19176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3953C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.973C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+111C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.546C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*453C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.529C>T
  hgvsp: ENSP00000453732.1:p.Thr177Ile
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+111C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.628C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.641C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+111C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+111C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+111C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+111C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr177Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

15-85189305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189305
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189305
    reference: chr 15
allele count: 1
allele frequency: 5.112474437627812e-5
allele num: 19560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.528A>G
  hgvsp: ENSP00000453732.1:p.Thr177Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+110A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.545A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+110A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.972A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+110A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.640A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3952A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.627A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+110A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+110A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*452A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+110A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr177Ala
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

15-85189316-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189316
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189316
    reference: chr 15
allele count: 3
allele frequency: 1.239976853765396e-4
allele num: 24194
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+99G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517G>C
  hgvsp: ENSP00000453732.1:p.Gly173Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.961G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.616G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+99G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+99G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+99G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+99G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3941G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.629G>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+99G>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly173Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

15-85189323-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189323
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189321
    reference: chr 15
allele count: 7
allele frequency: 2.466351913184413e-4
allele num: 28382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-9_*441-8delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+90_1023+91delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+90_981+91delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-9_534-8delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-9_517-8delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.607_608delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+90_1105+91delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.952_953delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.620_621delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3932_3933delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+90_593+91delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+90_*164+91delCT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+90_517+91delCT
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9679
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.534-9_534-8delCT
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: CAG
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

15-85189330-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189330
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189330
    reference: chr 15
allele count: 45
allele frequency: 1.304726007538417e-3
allele num: 34490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-14A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.947A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+85A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+85A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3927A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+85A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+85A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+85A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-14A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.615A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+85A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.602A>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-14A>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35746
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

15-85189330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189330
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189330
    reference: chr 15
allele count: 2
allele frequency: 5.798782255726298e-5
allele num: 34490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.602A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3927A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-14A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+85A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-14A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+85A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+85A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+85A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.947A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-14A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.615A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+85A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+85A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

15-85189336-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189336
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189334
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 41024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.607_608delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+77_*164+78delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+77_593+78delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3919_3920delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-22_517-21delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+77_981+78delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.594_595delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.939_940delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-22_*441-21delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+77_1023+78delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-22_534-21delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+77_517+78delTG
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+77_1105+78delTG
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34499
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: TCA
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-85189337-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189337
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189338
    reference: chr 15
allele count: 1
allele frequency: 2.379139703083365e-5
allele num: 42032
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-22dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3919dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+77dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+77dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.594dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-22dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.607dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+77dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-22dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.939dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+77dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+77dupT
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+77dupT
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

15-85189347-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189347
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189347
    reference: chr 15
allele count: 1
allele frequency: 1.882955486932289e-5
allele num: 53108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.598T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+68T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.930T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-31T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-31T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+68T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.585T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+68T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3910T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-31T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+68T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+68T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+68T>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

15-85189355-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189355
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189355
    reference: chr 15
allele count: 69
allele frequency: 1.04767689037352e-3
allele num: 65860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+60T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+60T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+60T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.577T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3902T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-39T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+60T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-39T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-39T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.922T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.590T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+60T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+60T>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23279
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20700
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

15-85189356-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189356
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189356
    reference: chr 15
allele count: 1
allele frequency: 1.408847562693717e-5
allele num: 70980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+59C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3901C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+59C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.589C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-40C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+59C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.576C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-40C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.921C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+59C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+59C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+59C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-40C>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

15-85189357-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189357
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189357
    reference: chr 15
allele count: 1
allele frequency: 1.398444929238687e-5
allele num: 71508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.920A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.588A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.575A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+58A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+58A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-41A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+58A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3900A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-41A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+58A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+58A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+58A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-41A>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22075
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

15-85189363-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189363
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189362
    reference: chr 15
allele count: 3
allele frequency: 3.75685626267939e-5
allele num: 79854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.568delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+51delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3893delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+51delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.581delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-48delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-48delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+51delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-48delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+51delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.913delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+51delC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+51delC
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23949
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18086
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: TG
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-85189363-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189363
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189364
    reference: chr 15
allele count: 3
allele frequency: 3.75685626267939e-5
allele num: 79854
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.517-48dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3893dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.534-48dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*441-48dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+51dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+51dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.913dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.581dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+51dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+51dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+51dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+51dupC
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.568dupC
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18086
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23949
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

15-85189377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189377
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189377
    reference: chr 15
allele count: 1
allele frequency: 1.025893553284911e-5
allele num: 97476
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3880C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.568C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.555C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.900C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+38C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+38C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-85189383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189383
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189383
    reference: chr 15
allele count: 10
allele frequency: 9.796430180842101e-5
allele num: 102078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3874T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.562T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.894T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.549T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+32T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+32T>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31022
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11176
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

15-85189395-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189395
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189395
    reference: chr 15
allele count: 1
allele frequency: 8.901865831078194e-6
allele num: 112336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.537C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.882C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.550C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3862C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+20C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+20C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

15-85189396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189396
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189396
    reference: chr 15
allele count: 2
allele frequency: 1.775915040224476e-5
allele num: 112618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.536C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.549C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3861C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+19C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.881C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

15-85189396-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189396
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189396
    reference: chr 15
allele count: 5
allele frequency: 4.439787600561189e-5
allele num: 112618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3861C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.881C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.549C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+19C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.536C>A
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35788
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-85189400-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189400
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189400
    reference: chr 15
allele count: 24
allele frequency: 2.108222066057625e-4
allele num: 113840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3857T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.877T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.545T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+15T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.532T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+15T>C
  variant of: http://identifiers.org/hgnc/25928
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12900
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-85189409-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189409
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189409
    reference: chr 15
allele count: 2
allele frequency: 1.729445539759953e-5
allele num: 115644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.523G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.868G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3848G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+6G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.536G>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13466
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.517+6G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

15-85189409-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189409
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189409
    reference: chr 15
allele count: 5
allele frequency: 4.323613849399883e-5
allele num: 115644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.868G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.536G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+6G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3848G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.523G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13466
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.517+6G>A
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

15-85189410-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189410
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189410
    reference: chr 15
allele count: 3
allele frequency: 2.587589918749676e-5
allele num: 115938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.981+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.533+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.535C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*164+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.516+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1105+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3847C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.522C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.593+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*440+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.867C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1023+5C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.517+5C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.517+5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

15-85189419-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189419
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189419
    reference: chr 15
allele count: 1
allele frequency: 8.505715841045183e-6
allele num: 117568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.523C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.858C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*160C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1019C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.529C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.512C>T
  hgvsp: ENST00000558521.1:c.512C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3838C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*436C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.513C>T
  hgvsp: ENST00000434634.2:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.513C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.526C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.977C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.589C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1101C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr171Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ

15-85189420-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189420
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189420
    reference: chr 15
allele count: 1
allele frequency: 8.498342823149486e-6
allele num: 117670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.857C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.512C>A
  hgvsp: ENSP00000387982.2:p.Thr171Asn
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.528C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1018C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.976C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.511C>A
  hgvsp: ENSP00000453732.1:p.Thr171Asn
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3837C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.525C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*435C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*159C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1100C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.522C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.588C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.512C>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr171Asn
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-85189423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189423
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189423
    reference: chr 15
allele count: 1
allele frequency: 8.477737461426295e-6
allele num: 117956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1015A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.509A>G
  hgvsp: ENSP00000387982.2:p.Tyr170Cys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.508A>G
  hgvsp: ENSP00000453732.1:p.Tyr170Cys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3834A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.519A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1097A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.854A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.585A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.522A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.525A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.509A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*432A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.973A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37487
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr170Cys
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-85189425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189425
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189425
    reference: chr 15
allele count: 12
allele frequency: 1.016036441840381e-4
allele num: 118106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.852G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.506G>A
  hgvsp: ENST00000558521.1:c.506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3832G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1013G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.520G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.507G>A
  hgvsp: ENST00000434634.2:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.507G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.583G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*154G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*430G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.971G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.523G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.517G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14277
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr169Thr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

15-85189426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189426
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189426
    reference: chr 15
allele count: 1
allele frequency: 8.454657670910904e-6
allele num: 118278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1012C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.970C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.522C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*153C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*429C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.582C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.851C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.506C>T
  hgvsp: ENSP00000387982.2:p.Thr169Met
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.519C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.505C>T
  hgvsp: ENSP00000453732.1:p.Thr169Met
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1094C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.506C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3831C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.516C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr169Met
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

15-85189427-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189427
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189427
    reference: chr 15
allele count: 1
allele frequency: 8.446373971653969e-6
allele num: 118394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*428A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.581A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.850A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.969A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.505A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.521A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1011A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.515A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1093A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.518A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.504A>G
  hgvsp: ENSP00000453732.1:p.Thr169Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3830A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.505A>G
  hgvsp: ENSP00000387982.2:p.Thr169Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*152A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr169Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

15-85189430-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189430
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189430
    reference: chr 15
allele count: 1
allele frequency: 8.429002511842749e-6
allele num: 118638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1008A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1090A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.966A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.502A>G
  hgvsp: ENSP00000387982.2:p.Thr168Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.502A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.515A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.518A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.501A>G
  hgvsp: ENSP00000453732.1:p.Thr168Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3827A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*149A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*425A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.578A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.847A>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.512A>G
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr168Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

15-85189435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189435
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189435
    reference: chr 15
allele count: 7
allele frequency: 5.887399283419401e-5
allele num: 118898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1085G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.842G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.497G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3822G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.496G>A
  hgvsp: ENSP00000453732.1:p.Arg166Gln
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*420G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.507G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.497G>A
  hgvsp: ENSP00000387982.2:p.Arg166Gln
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.573G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1003G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.513G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.510G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.961G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg166Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

15-85189436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189436
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189436
    reference: chr 15
allele count: 6
allele frequency: 5.04142369805233e-5
allele num: 119014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1084C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*419C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.496C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3821C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.960C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.496C>T
  hgvsp: ENSP00000387982.2:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.506C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1002C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.495C>T
  hgvsp: ENSP00000453732.1:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.509C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.841C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.512C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.572C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166Trp
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

15-85189437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189437
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189437
    reference: chr 15
allele count: 1
allele frequency: 8.396164631996104e-6
allele num: 119102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*418C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3820C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.494C>T
  hgvsp: ENST00000558521.1:c.494C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1083C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.495C>T
  hgvsp: ENST00000434634.2:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.511C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.840C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.959C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.571C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.495C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1001C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.508C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.505C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser165Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

15-85189438-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189438
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189438
    reference: chr 15
allele count: 1
allele frequency: 8.391655337931961e-6
allele num: 119166
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.494C>G
  hgvsp: ENSP00000387982.2:p.Ser165Cys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.507C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.504C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1082C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.570C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3819C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.493C>G
  hgvsp: ENSP00000453732.1:p.Ser165Cys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.1000C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*417C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*141C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.839C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.510C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.494C>G
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.958C>G
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser165Cys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

15-85189445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189445
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189445
    reference: chr 15
allele count: 1
allele frequency: 8.372404554588077e-6
allele num: 119440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*410C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.500C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.487C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.486C>T
  hgvsp: ENST00000558521.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.951C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.503C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.487C>T
  hgvsp: ENST00000434634.2:c.487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.832C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3812C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.497C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*134C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1075C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.563C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.993C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu163Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-85189450-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189450
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189450
    reference: chr 15
allele count: 1
allele frequency: 8.365960579593749e-6
allele num: 119532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.482T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1070T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.482T>C
  hgvsp: ENSP00000387982.2:p.Val161Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.827T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.481T>C
  hgvsp: ENSP00000453732.1:p.Val161Ala
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*129T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3807T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.492T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.988T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.498T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*405T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.946T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.558T>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.495T>C
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14780
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val161Ala
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

15-85189451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189451
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189451
    reference: chr 15
allele count: 4
allele frequency: 3.345824411134904e-5
allele num: 119552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.491G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3806G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.497G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.480G>A
  hgvsp: ENSP00000453732.1:p.Val161Ile
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*128G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.481G>A
  hgvsp: ENSP00000387982.2:p.Val161Ile
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1069G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.494G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*404G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.481G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.987G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.557G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.826G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.945G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val161Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-85189452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189452
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189452
    reference: chr 15
allele count: 24
allele frequency: 2.007393900868198e-4
allele num: 119558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.944C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3805C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.825C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.556C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.496C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.480C>T
  hgvsp: ENST00000434634.2:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*127C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.480C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.479C>T
  hgvsp: ENST00000558521.1:c.479C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.986C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1068C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.490C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.493C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*403C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37412
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val160Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-85189454-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189454
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189454
    reference: chr 15
allele count: 1
allele frequency: 8.359945827551038e-6
allele num: 119618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.942G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*401G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.478G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*125G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.488G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.491G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.554G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.823G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.477G>T
  hgvsp: ENSP00000453732.1:p.Val160Phe
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.478G>T
  hgvsp: ENSP00000387982.2:p.Val160Phe
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1066G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.494G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.984G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3803G>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37421
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val160Phe
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

15-85189457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189457
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189457
    reference: chr 15
allele count: 3
allele frequency: 2.507145364288222e-5
allele num: 119658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.939C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*398C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.491C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.475C>T
  hgvsp: ENSP00000387982.2:p.Gln159Ter
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.551C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3800C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*122C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1063C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.488C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.820C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.475C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.981C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.474C>T
  hgvsp: ENSP00000453732.1:p.Gln159Ter
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.485C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln159Ter
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

15-85189457-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189457
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189457
    reference: chr 15
allele count: 1
allele frequency: 8.357151214294072e-6
allele num: 119658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.475C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.474C>A
  hgvsp: ENSP00000453732.1:p.Gln159Lys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1063C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3800C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.551C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*398C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.981C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.820C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.488C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.475C>A
  hgvsp: ENSP00000387982.2:p.Gln159Lys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.939C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.491C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*122C>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.485C>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln159Lys
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

15-85189458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189458
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189458
    reference: chr 15
allele count: 1
allele frequency: 8.355614973262032e-6
allele num: 119680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.487G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3799G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.938G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.473G>A
  hgvsp: ENST00000558521.1:c.473G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.474G>A
  hgvsp: ENST00000434634.2:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1062G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.550G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*121G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.819G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.490G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*397G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.474G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.980G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.484G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu158Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

15-85189464-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189464
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189464
    reference: chr 15
allele count: 27515
allele frequency: 2.294293242612234e-1
allele num: 119928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.478A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.932A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.467A>C
  hgvsp: ENST00000558521.1:c.467A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.481A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*391A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1056A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*115A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3793A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.544A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.468A>C
  hgvsp: ENST00000434634.2:c.468A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.484A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.974A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.468A>C
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.813A>C
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 2145
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.25e1
  variant carriers: 1430
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 6.75e1
  variant carriers: 1721
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.25e1
  variant carriers: 2301
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.75e1
  variant carriers: 759
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 7.75e1
  variant carriers: 1169
genotype depth: GenotypeDepth
  all individuals: 9764
  bin: 2.75e1
  variant carriers: 552
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 9.75e1
  variant carriers: 3253
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 3.75e1
  variant carriers: 1370
genotype depth: GenotypeDepth
  all individuals: 22669
  bin: 2.25e1
  variant carriers: 332
genotype quality: GenotypeQuality
hgvs: p.Arg156Arg
num of homozygotes: 3491
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/15-85189465-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189465
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189465
    reference: chr 15
allele count: 2
allele frequency: 1.667139022723105e-5
allele num: 119966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.812G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.973G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.467G>T
  hgvsp: ENSP00000387982.2:p.Arg156Leu
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3792G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.543G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.931G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.466G>T
  hgvsp: ENSP00000453732.1:p.Arg156Leu
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*390G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.480G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.483G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.467G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*114G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.477G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1055G>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg156Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

15-85189465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189465
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189465
    reference: chr 15
allele count: 1
allele frequency: 8.335695113615524e-6
allele num: 119966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.483G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.466G>A
  hgvsp: ENSP00000453732.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.467G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.467G>A
  hgvsp: ENSP00000387982.2:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.812G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*390G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1055G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.931G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.480G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3792G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.477G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.973G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.543G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg156Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

15-85189466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189466
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189466
    reference: chr 15
allele count: 1
allele frequency: 8.333194446759221e-6
allele num: 120002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.972C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.479C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3791C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.466C>T
  hgvsp: ENSP00000387982.2:p.Arg156Ter
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.930C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.465C>T
  hgvsp: ENSP00000453732.1:p.Arg156Ter
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*389C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.482C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*113C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.811C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.542C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.476C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1054C>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.466C>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg156Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

15-85189471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189471
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189471
    reference: chr 15
allele count: 1
allele frequency: 8.330556481172942e-6
allele num: 120040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.537G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.461G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3786G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.925G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.477G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.474G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1049G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.460G>A
  hgvsp: ENSP00000453732.1:p.Arg154Lys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*384G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.461G>A
  hgvsp: ENSP00000387982.2:p.Arg154Lys
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*108G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.471G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.806G>A
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.967G>A
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg154Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-85189473-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85189473
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85189473
    reference: chr 15
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559015
  gene symbol: WDR73
  hgvsc: ENST00000559015.1:n.1047G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000387982
  ensembl transcript: ENST00000434634
  gene symbol: WDR73
  hgvsc: ENST00000434634.2:c.459G>T
  hgvsp: ENST00000434634.2:c.459G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560966
  gene symbol: WDR73
  hgvsc: ENST00000560966.1:n.3784G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000398528
  gene symbol: WDR73
  hgvsc: ENST00000398528.3:n.535G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000558608
  gene symbol: WDR73
  hgvsc: ENST00000558608.1:n.804G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000561329
  gene symbol: WDR73
  hgvsc: ENST00000561329.1:n.459G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453732
  ensembl transcript: ENST00000558521
  gene symbol: WDR73
  hgvsc: ENST00000558521.1:c.458G>T
  hgvsp: ENST00000558521.1:c.458G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560835
  gene symbol: WDR73
  hgvsc: ENST00000560835.1:n.475G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559126
  gene symbol: WDR73
  hgvsc: ENST00000559126.1:n.965G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000560088
  gene symbol: WDR73
  hgvsc: ENST00000560088.1:n.469G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559994
  gene symbol: WDR73
  hgvsc: ENST00000559994.1:n.472G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453204
  ensembl transcript: ENST00000559178
  gene symbol: WDR73
  hgvsc: ENST00000559178.1:c.*382G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177082
  ensembl protein: ENSP00000453779
  ensembl transcript: ENST00000559224
  gene symbol: WDR73
  hgvsc: ENST00000559224.1:c.*106G>T
  variant of: http://identifiers.org/hgnc/25928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177082
  ensembl transcript: ENST00000559452
  gene symbol: WDR73
  hgvsc: ENST00000559452.1:n.923G>T
  variant of: http://identifiers.org/hgnc/25928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala153Ala
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 53
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5315
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 307
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 643
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14099
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.345558838866679e-5
allele num: 23012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.93e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.116e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.333e0

VQSLOD
type: SiteQuality
SIO_000300: -1.517e0

QD
type: SiteQuality
SIO_000300: 5.02e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

GenotypeQuality
all individuals: 1043
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21366
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2370
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23561
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4545
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 358
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2486
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.225806451612903e-3
allele num: 310
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.27e-2

DP
type: SiteQuality
SIO_000300: 5.29676e5

QD
type: SiteQuality
SIO_000300: 8.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

GenotypeQuality
all individuals: 1899
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2745
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28830
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 13736
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 4.34918e5

VQSLOD
type: SiteQuality
SIO_000300: -7.849e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.88e-2

QD
type: SiteQuality
SIO_000300: 1.053e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeQuality
all individuals: 4199
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29449
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1821
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13271
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1396
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.256281407035176e-4
allele num: 7960
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1004
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.99e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.141e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.332e0

QD
type: SiteQuality
SIO_000300: 1.239e1

DP
type: SiteQuality
SIO_000300: 4.27628e5

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7818
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1264
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.514e0

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.88e-1

DP
type: SiteQuality
SIO_000300: 4.12207e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.72e0

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
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allele count: 5
allele frequency: 4.032258064516129e-3
allele num: 1240
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7622
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 4.07248e5

VQSLOD
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SIO_000300: -1.198e0

ReadPosRankSum
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SIO_000300: 4.21e-1

MQRankSum
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FS
type: SiteQuality
SIO_000300: 4.984e0

ClippingRankSum
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SIO_000300: -3.06e-1

QD
type: SiteQuality
SIO_000300: 1.529e1

BaseQRankSum
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SIO_000300: 1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.34e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1154
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6968
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.55e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -7.2e-1

ReadPosRankSum
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SIO_000300: 1.38e0

VQSLOD
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SIO_000300: -2.042e0

DP
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SIO_000300: 3.93831e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e0

QD
type: SiteQuality
SIO_000300: 1.192e1

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: 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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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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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.62813415825464e-4
allele num: 6142
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.65307e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
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SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.89e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.664e0

VQSLOD
type: SiteQuality
SIO_000300: -9.416e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

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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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 1.303101381287464e-4
allele num: 7674
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 996
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

DP
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.896e1

BaseQRankSum
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FS
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SIO_000300: 0.0e0

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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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5714
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 396
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South Asian
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num of homozygotes: 0

MQRankSum
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SIO_000300: -3.58e-1

ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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SIO_000300: 1.23e0

FS
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ClippingRankSum
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VQSLOD
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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: 682
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5518
num of homozygotes: 0

African
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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MQ
type: SiteQuality
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FS
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QD
type: SiteQuality
SIO_000300: 4.04e0

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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South Asian
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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MQRankSum
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FS
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MQ
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DP
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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FS
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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FS
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DP
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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Latino
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Other
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Latino
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European (Non-Finnish)
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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DP
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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African
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East Asian
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South Asian
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MQ
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.534854245880862e-4
allele num: 7890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
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SIO_000300: -4.17e-2

MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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SIO_000300: 8.45e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

FS
type: SiteQuality
SIO_000300: 9.055999999999999e0

BaseQRankSum
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SIO_000300: -3.364e0

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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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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1286
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.207729468599034e-4
allele num: 8280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.66363e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.03e-2

QD
type: SiteQuality
SIO_000300: 7.35e0

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
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SIO_000300: 2.93e0

ClippingRankSum
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SIO_000300: -1.67e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: -1.444e0

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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GenotypeQuality
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variant carriers: 3

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1020
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.632840881569387e-4
allele num: 8258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.33688e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e-1

ClippingRankSum
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SIO_000300: -1.62e-1

QD
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SIO_000300: 1.205e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -2.87e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 116
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 4.309106578569377e-4
allele num: 13924
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1888
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.429420505200594e-4
allele num: 1346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

QD
type: SiteQuality
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FS
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SIO_000300: 1.943e0

InbreedingCoeff
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SIO_000300: -2.35e-2

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.79855e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 39

African
type: Population
allele count: 2
allele frequency: 8.598452278589854e-4
allele num: 2326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.233638597274961e-4
allele num: 8954
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 6.738544474393531e-4
allele num: 1484
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 40
allele frequency: 2.22543674196061e-3
allele num: 17974
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
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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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SIO_000300: 4.25e0

DP
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QD
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BaseQRankSum
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SIO_000300: 9.22e-1

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: 2

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 1.112718370980305e-4
allele num: 17974
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

East Asian
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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: 8954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1484
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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QD
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ClippingRankSum
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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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22290
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 1966
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2770
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 6.92014e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.159e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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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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bin: 1.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 11725
bin: 6.25e1
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GenotypeQuality
all individuals: 950
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2102
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 3.506311360448808e-4
allele num: 2852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2042
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22932
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.607e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

MQRankSum
type: SiteQuality
SIO_000300: -9.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.02356e5

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 65
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29820
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.794857462269424e-4
allele num: 3578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3134
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2770
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e-1

DP
type: SiteQuality
SIO_000300: 7.96251e5

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

GenotypeDepth
all individuals: 5450
bin: 1.25e1
variant carriers: 29

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2419
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variant carriers: 27

GenotypeQuality
all individuals: 583
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variant carriers: 2

GenotypeQuality
all individuals: 711
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variant carriers: 7

GenotypeQuality
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bin: 4.25e1
variant carriers: 6

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 550
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variant carriers: 6

GenotypeQuality
all individuals: 1708
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2021
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variant carriers: 2

GenotypeQuality
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variant carriers: 12

GenotypeQuality
all individuals: 1026
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 104
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2089
bin: 6.75e1
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GenotypeQuality
all individuals: 21178
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variant carriers: 7

GenotypeQuality
all individuals: 554
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variant carriers: 1

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 1.156722440415344e-3
allele num: 37174
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.302925989672978e-4
allele num: 4648
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 2.501136880400182e-3
allele num: 4398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 3.409795412275264e-3
allele num: 3226
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.99203187250996e-3
allele num: 502
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4390
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.929e0

VQSLOD
type: SiteQuality
SIO_000300: -9.342000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

QD
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 4.1873e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.21189e5

MQ
type: SiteQuality
SIO_000300: 5.845e1

GenotypeDepth
all individuals: 2192
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeDepth
all individuals: 0
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GenotypeQuality
all individuals: 2044
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variant carriers: 0

GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 502
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GenotypeQuality
all individuals: 1975
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GenotypeQuality
all individuals: 22295
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GenotypeQuality
all individuals: 389
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GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 1107
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GenotypeQuality
all individuals: 2547
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GenotypeQuality
all individuals: 23561
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GenotypeQuality
all individuals: 594
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variant carriers: 0

GenotypeQuality
all individuals: 1842
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GenotypeQuality
all individuals: 97
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 391
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GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 663
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GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.01450443190975e-4
allele num: 4964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.33178e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
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SIO_000300: -3.297e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 0
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GenotypeDepth
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GenotypeQuality
all individuals: 104
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22386
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.473043822336532e-5
allele num: 40436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3876
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.42781e5

FS
type: SiteQuality
SIO_000300: 3.3525e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.424e0

QD
type: SiteQuality
SIO_000300: 3.74e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQ
type: SiteQuality
SIO_000300: 5.177e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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bin: 6.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 2.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.642752756742394e-5
allele num: 45162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6244
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.018498e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

QD
type: SiteQuality
SIO_000300: 5.12e0

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
all individuals: 5230
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GenotypeDepth
all individuals: 0
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GenotypeQuality
all individuals: 2870
bin: 6.75e1
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GenotypeQuality
all individuals: 540
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GenotypeQuality
all individuals: 634
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 7.5e0
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 420
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 1.75e1
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GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
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GenotypeQuality
all individuals: 937
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 19127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24532
bin: 6.25e1
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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African
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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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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European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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Other
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MQRankSum
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FS
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DP
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InbreedingCoeff
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QD
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MQ
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 5162
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South Asian
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European (Non-Finnish)
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African
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Latino
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Other
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East Asian
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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MQRankSum
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VQSLOD
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FS
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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European (Finnish)
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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FS
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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Other
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South Asian
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East Asian
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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DP
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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MQ
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DP
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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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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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.140210394096405e-5
allele num: 63690
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
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
allele num: 6440
num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

MQRankSum
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FS
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DP
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InbreedingCoeff
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SIO_000300: 1.9e-3

ClippingRankSum
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ReadPosRankSum
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SIO_000300: -8.0e-2

BaseQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8832
num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 2.469135802469136e-4
allele num: 16200
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.570105197048202e-5
allele num: 63690
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.132930229643786e-5
allele num: 63838
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.16370808678501e-5
allele num: 16224
num of homozygotes: 0

MQRankSum
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SIO_000300: -6.4e-1

ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 1.409097e6

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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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
allele num: 8486
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.544640098856966e-5
allele num: 64740
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -3.193e0

VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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QD
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FS
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SIO_000300: 8.196999999999999e0

MQ
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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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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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South Asian
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African
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East Asian
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allele num: 8490
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
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Latino
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European (Non-Finnish)
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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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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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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South Asian
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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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num of homozygotes: 0

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

Other
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South Asian
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allele count: 9
allele frequency: 5.4931640625e-4
allele num: 16384
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Latino
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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InbreedingCoeff
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Finnish)
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Other
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African
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Latino
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65372
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South Asian
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Latino
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African
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Other
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BaseQRankSum
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SIO_000300: 3.99e0

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

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

African
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allele num: 9620
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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MQ
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FS
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QD
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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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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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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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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African
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Other
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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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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African
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Latino
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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MQ
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MQRankSum
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DP
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819063788503517e-4
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65954
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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

QD
type: SiteQuality
SIO_000300: 1.621e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.43e-2

FS
type: SiteQuality
SIO_000300: 1.023e0

ReadPosRankSum
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SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.208e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516208266367468e-5
allele num: 65954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.208e0

QD
type: SiteQuality
SIO_000300: 1.621e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.43e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

FS
type: SiteQuality
SIO_000300: 1.023e0

DP
type: SiteQuality
SIO_000300: 1.463312e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

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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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 614
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variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515840533575868e-5
allele num: 65970
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.729e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.463639e6

QD
type: SiteQuality
SIO_000300: 1.389e1

GenotypeDepth
all individuals: 535
bin: 9.25e1
variant carriers: 533

GenotypeDepth
all individuals: 275
bin: 1.25e1
variant carriers: 104

GenotypeDepth
all individuals: 947
bin: 8.25e1
variant carriers: 945

GenotypeDepth
all individuals: 2376
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variant carriers: 2350

GenotypeDepth
all individuals: 4137
bin: 3.25e1
variant carriers: 920

GenotypeDepth
all individuals: 1940
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variant carriers: 1783

GenotypeDepth
all individuals: 2188
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variant carriers: 2167

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 15

GenotypeQuality
all individuals: 507
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variant carriers: 57

GenotypeQuality
all individuals: 4753
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variant carriers: 36

GenotypeQuality
all individuals: 78
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variant carriers: 3

GenotypeQuality
all individuals: 82
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variant carriers: 6

GenotypeQuality
all individuals: 50
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variant carriers: 2

GenotypeQuality
all individuals: 99
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variant carriers: 14

GenotypeQuality
all individuals: 393
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variant carriers: 11

GenotypeQuality
all individuals: 19
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variant carriers: 8

GenotypeQuality
all individuals: 108
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variant carriers: 13

GenotypeQuality
all individuals: 30
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variant carriers: 9

GenotypeQuality
all individuals: 159
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GenotypeQuality
all individuals: 24003
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variant carriers: 23589

GenotypeQuality
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variant carriers: 71

GenotypeQuality
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bin: 7.25e1
variant carriers: 34

GenotypeQuality
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variant carriers: 32

GenotypeQuality
all individuals: 1314
bin: 8.25e1
variant carriers: 64

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 14

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 24

GenotypeQuality
all individuals: 2026
bin: 7.75e1
variant carriers: 43

European (Finnish)
type: Population
allele count: 1726
allele frequency: 2.613567534827377e-1
allele num: 6604
num of homozygotes: 222

Latino
type: Population
allele count: 2018
allele frequency: 1.751128080527595e-1
allele num: 11524
num of homozygotes: 178

East Asian
type: Population
allele count: 1141
allele frequency: 1.331699346405229e-1
allele num: 8568
num of homozygotes: 85

Other
type: Population
allele count: 218
allele frequency: 2.460496613995485e-1
allele num: 886
num of homozygotes: 30

African
type: Population
allele count: 596
allele frequency: 6.167218543046358e-2
allele num: 9664
num of homozygotes: 18

European (Non-Finnish)
type: Population
allele count: 18548
allele frequency: 2.802659413720157e-1
allele num: 66180
num of homozygotes: 2576

South Asian
type: Population
allele count: 3268
allele frequency: 1.980366016240456e-1
allele num: 16502
num of homozygotes: 382

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

FS
type: SiteQuality
SIO_000300: 5.26e-1

QD
type: SiteQuality
SIO_000300: 1.767e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 2.494682e6

GenotypeDepth
all individuals: 11907
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 252
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variant carriers: 0

GenotypeDepth
all individuals: 2785
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 377
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variant carriers: 0

GenotypeDepth
all individuals: 547
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GenotypeDepth
all individuals: 2919
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GenotypeQuality
all individuals: 1674
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GenotypeQuality
all individuals: 208
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 149
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 150
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GenotypeQuality
all individuals: 140
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66180
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
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VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
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SIO_000300: -2.81e-1

BaseQRankSum
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SIO_000300: -1.024e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

DP
type: SiteQuality
SIO_000300: 2.034708e6

QD
type: SiteQuality
SIO_000300: 1.145e1

GenotypeDepth
all individuals: 93
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2530
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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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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: 150
bin: 3.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.0351966873706e-4
allele num: 9660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66180
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.034708e6

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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
all individuals: 1671
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GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510345869204048e-5
allele num: 66210
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 1.022e0

DP
type: SiteQuality
SIO_000300: 2.034877e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.091e0

QD
type: SiteQuality
SIO_000300: 2.89e1

VQSLOD
type: SiteQuality
SIO_000300: -1.275e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeDepth
all individuals: 2788
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2853
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1213
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2920
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1620
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2304
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5983
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14857
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1671
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

DP
type: SiteQuality
SIO_000300: 2.035394e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.212e0

QD
type: SiteQuality
SIO_000300: 2.299e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.805e0

GenotypeDepth
all individuals: 11979
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 786
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 518
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2856
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 252
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27830
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0